LICENSE AGREEMENT

 

           THIS LICENSE AGREEMENT (this “Agreement”) is made as of March 19, 2010 (the “Effective Date”), by and among Svelte Medical Systems, Inc., a Delaware corporation having its principal place of business at 657 Central Avenue, New Providence, New Jersey 07974 (collectively, “Licensor”), and Inspire/MD Ltd., an Israeli corporation, having its principal place of business at 3 Menorat Hamaor St., Tel Aviv, Israel (“Licensee”).  Licensor and Licensee are each individually referred to herein without distinction as a “Party” and collectively as the “Parties.”

 

 

Licensor is a medical device company engaged in the discovery and development of medical devices using its proprietary stent-on-a-wire stent delivery system and solely owns all worldwide right, title and interest in and to the Svelte helical stent ("SHS"), which specifications are as set forth in Exhibit A attached hereto, which is the subject (at least in part)  of those certain patents and patent applications set forth on Exhibit B, attached hereto, which are also the sole property of Licensor.

 

Licensee desires to obtain from Licensor, and Licensor is willing to grant Licensee, a non-exclusive license to the SHS, the above identified patents and related technology on the terms and conditions set forth herein.

 

 

Now, Therefore, in consideration of the foregoing and the terms, conditions and covenants hereinafter set forth, Licensor and Licensee hereby agree as follows:

 

 

Capitalized terms used herein and not otherwise defined shall have the following meanings:

 

1.1           “Affiliate” means each and every business entity controlling, controlled by or under common control with a Party.  For purposes of this definition, “control” shall mean ownership, directly or indirectly, of more than fifty percent (50%) of the voting or income interest of the applicable business entity.

 

 

1.2           “Confidential Information” means any information disclosed by a Party (the “Disclosing Party”) to the other Party (the “Receiving Party”), including, without limitation, trade secrets, documents expressly designated as confidential, information related to either Party’s design, drawings, development or manufacturing processes, products, devices, employees, facilities, equipment, security systems, information systems, finances, product plans, marketing plans, suppliers, or distributors and all confidential regulatory applications, regulatory and clinical materials and related filings, applications and data, the content of any unpublished patent applications, operating methods and procedures, marketing, manufacturing, distribution and sales methods and systems, sales figures, pricing policies and price lists and other business information and shall include all confidential information disclosed or accessed by the parties pursuant to the provisions of this Agreement.  “Confidential Information” shall not include information that (a) is now available or becomes available to the public without breach of this Agreement; (b) is explicitly approved for release by written authorization of the Disclosing Party; (c) is lawfully obtained from a third party or parties without a duty of confidentiality; (d); is known to the Receiving Party prior to disclosure as evidenced by prior written records; or (e) is at any time developed by or for the Receiving Party independently of any such disclosure(s) from the Disclosing Party as evidenced by prior written records.

 

1.3           “Damages” shall mean any and all costs, losses, claims, liabilities, fines, penalties, damages and expenses, court costs, and reasonable fees and disbursements of counsel, consultants and expert witnesses incurred by a Party hereto (including any interest payments which may be imposed in connection therewith).

 

1.4           “Improvements” means all present and future supplements, changes, derivatives, revisions, updates, advancements, inventions, corrections and modifications that are applicable to the manufacture or use of the Licensed Product or use of the Licensed Patent or Licensed Processes, whether developed or created by Licensor or Licensee.

 

1.5            “Intellectual Property” means (a) any inventions, ideas, discoveries, developments, improvements, innovations, and know-how, whether or not subject to patent, copyright or trademark protection; (b) trade secrets; (c) compositions of matter, (d) proprietary procedures, prototypes, products or devices; and (e) experimental and regulatory results.

 

1.6           “License” means the license granted under Section 2.1 hereof.

 

1.7           “Licensed Product” means Licensee’s RX stent delivery catheter with the SHS and Licensee’s mesh covering.

 

1.8           “Licensed Process(es)” means any process or method that is covered in whole or in part by an issued, unexpired claim or a pending claim contained in the Licensed Patents.

 

1.9           “Licensed Patents” shall mean all the patents and patent applications listed in Exhibit B attached hereto; (b) any international counterparts thereof; and (c) all patents issuing from any of the foregoing.

 

1.10           “Net Sales” shall mean the gross invoiced sales prices charged for all Licensed Products sold by Licensee to third parties for which Licensee actually received payment from such third parties less: (a) trade discounts (including without limitation discounts given to distributors, agents and representatives), prompt payment and quantity discounts actually given; (b) any tax imposed or other governmental charge (other than income tax) charged or levied on the sale, use, transportation, or delivery of the products and borne or passed through to Licensee; (c) credits or allowances actually given and arising from returned or rejected products or retrospective price adjustments to any such products and recalls; (d)   governmental and managed care rebates, and hospital or other buying group charge backs.

 

 

1.11           “Royalty Bearing Sale” means any sale, lease or transfer of any Licensed Product, by Licensee for which Licensee has received revenue.

 

1.12           “Territory” shall mean all of the countries and territories of the world.

 

 

2.1           License Grant.  Licensor hereby grants to Licensee a non-exclusive, world-wide license under the Licensed Patents and the Licensed Processes and any Improvements thereon made by Licensor, with the right to use, make, have made, (including the right to have a third party to manufacture the Licensed Products)sell, offer, distribute, market, import and export the Licensed Products and to otherwise practice the technology related to the SHS and the Licensed Patents and Licensed Processes, for the purposes of this Agreement as well as each component of or material or apparatus for use in making any Licensed Products in the Territory. Licensee shall have the sole right to determine the prices at which it sells Licensed Products in the Territory to any customer without any approval from Licensor.

 

2.2           Term.  Unless sooner terminated as provided in this Agreement, the License shall extend until the expiration, abandonment or invalidation of the last to expire, abandoned or invalidated of the Licensed Patents that is material to the License.

 

 

3.1           Regulatory Cost Sharing.  The Parties agree that all regulatory costs for receiving CE Mark for the Licensed Product shall be borne fifty percent (50%) by Licensee and fifty percent (50%) by Licensor; provided, however, that Licensor’s obligations under this Section 3.1 shall not exceed eighty five Thousand Dollars ($85,000).

 

All regulatory costs for receiving FDA Approval for conducting clinical trials, manufacture, distribute and sale for the Licensed Product shall be borne in equal portions by the Parties, provided however that Licensor's obligations under this Section 3.2 shall not exceed US$ 200,000 with no portion payable prior to completion of enrollment in the US IDE clinical trial.

 

 

(a)           Licensee shall pay Licensor a royalty in the aggregate amount of seven percent (7%) of Net Sales (the “Worldwide Royalty”) actually received by Licensee from the sale of any Licensed Product in any country other than the United States.

 

(b)           Licensee shall pay Licensor a royalty equal to the sum of (i) seven percent (7%) of the first US$ 10,000,000 of Net Sales resulting from the sale of any Licensed Product in the United States, and (ii) ten percent (10%) of Net Sales for all amounts of Net Sales resulting from the sale of any Licensed Product in the United States in excess of the first $ 10,000,000 of Net Sales (the “US Royalty”, together with the Worldwide Royalty, and without distinction between them, the “Royalty”).

 

 

3.3           Report.  Beginning in the first calendar quarter after the Effective Date in which there is a Royalty Bearing Sale, within forty-five (45) days after the close of each calendar quarter during the term of this Agreement, Licensee will submit to Licensor a written report which will show the total number of the Licensed Products as to which Royalty Bearing Sales were made during such quarter, the aggregate Net Sales received by Licensee during such quarter and the amount of Royalties payable to Licensor by Licensee under this Agreement for such quarter.

 

3.4           Payment and Audit.  Licensee shall pay the Royalty for each quarter to Licensor pursuant to Section 3.2 on a quarterly basis within sixty (60) days after the end of each quarter.  Sales made in foreign currency will be determined in the foreign funds for the country in which the Licensed Products are sold, and then converted into equivalent United States dollars at the rate of exchange for selling funds as published by the Wall Street Journal (or its successor publication) for the last business day prior to payment.  Upon reasonable notice to Licensee, Licensor shall have the right to have an independent certified public accountant (the “CPA”), selected by Licensor and reasonably acceptable to Licensee, audit Licensee’s records, during normal business hours, to verify the Royalties payable by Licensee to Licensor; provided, however, that such audit shall not take place more frequently than once a year and shall not cover such records for more than the preceding two (2) years.  The accountant shall only report to Licensor as to the accuracy of the payments paid by Licensee to Licensor, and in the event of any inaccuracy, the correct amount of such payment.  Licensee shall promptly pay to Licensor the amount of any underpayment determined in such audit.  Such audit shall be at Licensor’s expense unless the audit identifies greater than ten percent (10%) error, in which case such audit shall be at Licensee’s expense.  Licensee shall preserve and maintain all such records and accounts required for audit for a period of two (2) years after the calendar quarter for which the record applies. The CPA and Licensor shall be required to agree to keep all such financial and business information of Licensee being examined confidential and not disclose such information to any third party or use same for any purpose other than as contemplated in this Agreement; and, if so requested by Licensee, shall sign a confidentiality agreement prepared by Licensee for such purpose.

 

 

 

4.1           Prosecution and Maintenance.  Licensor has the right to control all aspects of filing, prosecuting, and maintaining all of the patents and patent applications that form the basis for the Licensed Patents, including foreign filings and patent cooperation treaty filings.  Licensee agrees to perform all actions and execute or cause to be executed all documents necessary to support such filing, prosecution or maintenance. Licensor shall: (i) keep Licensee reasonably informed as to the application for, prosecution of and maintenance of the forgoing patent application; (ii) furnish to Licensee copies of documents relevant to any such application, prosecution and maintenance; (iii) allow Licensee reasonable opportunity to comment on documents filed with any governmental entity that could affect the nature or scope of such patent applications or patent to be issued thereunder; and (iv) obtain Licensee’s consent prior to acting or refraining from acting in respect of prosecuting or maintaining any of the patent applications encompassed within the SHS.

 

4.2           Notice of Infringement.  Each Party shall promptly advise the other in writing of any (i) known acts of potential infringement of the Licensed Patents by any third party; and (ii) allegations that the SHS (or any part thereof) infringes on the rights of any third party.

 

 

(a)           Licensor has the first option to police the Licensed Patents against infringement by other parties within the Territory.  The right to police includes defending any action for declaratory judgment of non-infringement or invalidity; and prosecuting, defending or settling all infringement and declaratory judgment actions at its expense and through counsel of its selection.  Licensee shall provide reasonable assistance to Licensor with respect to such actions, but only if Licensor reimburses Licensee for expenses incurred in connection with any such assistance rendered at Licensor’s request.  Licensor shall defend, indemnify and hold harmless Licensee with respect to any counterclaims asserted by an alleged infringer reasonably related to the enforcement of the Licensed Patents under this Section, including, without limitation, antitrust counterclaims; provided, however that Licensor shall have no obligation to defend, indemnify or hold Licensee harmless with respect to any such counterclaim that arise from Licensee’s gross negligence or willful misconduct.  If Licensor undertakes to enforce and/or defend the Licensed Patents by litigation, Licensor shall pay all costs thereof and shall be entitled to all damages recovered in any such litigation. If within six (6) months after Licensor was first notified of such infringement, Licensor has not brought a suit against any third party referred to in this Section or caused such possible infringement to be discontinued on terms acceptable to Licensee, then Licensee shall have the right, in its sole discretion, but not the obligation, to bring suit against such third party, in Licensee’s name if possible.  Licensee shall bear all the expenses of any suit brought by Licensee and Licensee shall retain all damages or other monies awarded, or received in settlement of such suit (which amount shall be treated as Net Sales and subject to the Royalty) .  Licensor will cooperate with Licensee in any such suit being prosecuted by Licensee and shall take such actions and provide such assistance as Licensee shall request in connection with the prosecution of such suit including, but not limited to, being joined or otherwise named as a plaintiff in any such suit.

 

 

(b)           Upon becoming aware of any claim, counter-claim, demand or other action that is initiated, brought or threatened by a third party seeking to invalidate, reexamine or otherwise abrogate any of the Licensed  Patents, each Party shall each promptly notify the other in writing. Should Licensor elect not to defend one or more of the Licensed Patents against the claim, counter-claim, demand or other action, Licensor shall provide Licensee the opportunity in Licensee’s discretion to defend such claim, counter-claim, demand or other action, and Licensor will cooperate with Licensee in any such defense and shall take such actions and provide such assistance as Licensee shall request; provided, however, that Licensee shall directly bear all of its costs and expenses (including attorneys’ fees) pursuant to Licensee’s election to defend such action.

 

 

5.1           Corporate Existence and Power.  Each Party represents and warrants to the other that it (a) is a corporation duly organized, validly existing and in good standing under the laws of the state in which it is incorporated, and (b) has full corporate power and authority and the legal right to own and operate its property and assets and to carry on its business as it is now being conducted and is contemplated in this Agreement.

 

5.2           Authority.  Each Party represents and warrants to the other that it (a) has the requisite power and authority and the legal right to enter into this Agreement and perform its obligations hereunder; (b) has taken all necessary action on its part required to authorize the execution and delivery of the Agreement and the performance of its obligations hereunder; and (c) the Agreement has been duly executed and delivered on behalf of such Party, and constitutes a legal, valid and binding obligation of such Party and is enforceable against it in accordance with its terms.

 

5.3           Absence of Litigation.  Licensor represents and warrants to Licensee that: (i)  it is not aware of any pending or threatened litigation (and has not received any communication relating thereto) which alleges that Licensor’s activities, with respect to the Licensed Patents or otherwise related to this Agreement, have infringed or misappropriated, or that by conducting the activities as contemplated herein by Licensee would infringe or misappropriate, any of the intellectual property rights of any other person; (ii) it owns all worldwide rights, title and interests in and to the SHS (including the trademarks included therein), and the patents and patent applications listed in Exhibit B attached hereto and that the descriptions of the SHS set forth on Exhibit A hereto are true, correct and complete descriptions thereof; (iii) it is not aware  of any person or entity which is infringing, misappropriating or otherwise transgressing upon the SHS or  Licensed Patents; (iv) none of the intellectual property included within the SHS is invalid, unenforceable, or otherwise impaired such that it cannot be enjoyed to its purported full extent; (v) Exhibit A includes all technology and related intellectual property that is material to the manufacture and sale of the SHS as part of the Licensed Product; (vi) as of the Effective Date is not aware of any rights of any person or entity that are or could reasonably believed to be infringed by the making, using or selling of the SHS as part of the Licensed Product; and (vii) attached as Exhibit C is an executive summary prepared by Licensor's patent attorneys regarding the SHS.

 

 

5.4           No Approvals or Consents.  Except as otherwise described in this Agreement, each Party represents and warrants to the other that all necessary consents, approvals and authorizations of all governmental authorities and other persons or entities required to be obtained by such Party in connection with entry into this Agreement have been obtained.

 

5.5           No Conflict.  Each Party represents and warrants to the other that the execution and delivery of the Agreement by such Party and the performance of such Party’s obligations hereunder (a) do not conflict with or violate any requirement of applicable law or regulation or any provision of articles of incorporation or bylaws of such Party in any material way, and (b) do not conflict with, violate or breach or constitute a default or require any consent under, any contractual obligation or court or administrative order by which such Party is bound.

 

5.6           No Third Party IP. No Third Party Intellectual Property Rights are required for the exploitation of the License, including without limitation for the manufacture, distribution, sale or otherwise use of the Product set forth in Exhibit A.

 

 

6.1           Licensor’s Indemnity.  Licensor shall at all times during the term of this Agreement and thereafter indemnify, defend and hold Licensee (and its directors, officers, employees, and Affiliates) harmless from and against any and all Damages incurred or suffered by Licensee (and its directors, officers, employees, and Affiliates) (excluding incidental or consequential Damages suffered or incurred by Licensee directly (as opposed to incidental or consequential Damages suffered or incurred by third parties who are, in turn, seeking the same from Licensee, which shall be covered by the indemnity set forth herein)) as a consequence of third party claims or actions based upon:

 

(a)           any breach of any representation or warranty made by Licensor in this Agreement; or

 

(b)           any failure to perform duly and punctually any covenant, agreement or undertaking on the part of Licensor contained in this Agreement.

 

(c)           infringements or claims of infringements in relation to the SHS on any intellectual property rights of any other person.

 

(d)           the design of the SHS.

 

 

6.2           Licensee’s Indemnity.  Licensee shall at all time during the term of this Agreement and thereafter, indemnify, defend and hold Licensor (and its  directors, officers, employees, and Affiliates) harmless from and against any and all Damages incurred or suffered by Licensor (and its directors, officers, employees, and Affiliates) (excluding incidental or consequential Damages suffered or incurred by Licensor directly (as opposed to incidental or consequential Damages suffered or incurred by third parties who are, in turn, seeking the same from Licensor, which shall be covered by the indemnity set forth herein)) as a consequence of third party claims or actions based on:

 

(a)           any breach of any representation or warranty made by Licensee in this Agreement; or

 

(b)           any failure to perform duly and punctually any covenant, agreement or undertaking on the part of Licensee contained in this Agreement.

 

 

7.1           Termination.  Anything herein to the contrary notwithstanding, this Agreement may be terminated as follows:

 

(a)           Termination for Bankruptcy.  If either Licensee or Licensor (i) makes a general assignment for the benefit of creditors; (ii) files an insolvency petition in bankruptcy; (iii) petitions for or acquiesces in the appointment of any receiver, trustee or similar officer to liquidate or conserve its business or any substantial part of its assets; (iv) commences under the laws of any jurisdiction any proceeding involving its insolvency, bankruptcy, reorganization, adjustment of debt, dissolution, liquidation or any other similar proceeding for the release of financially distressed debtors; or (v) becomes a party to any proceeding or action of the type described above in (iii) or (iv) and such proceeding or action remains undismissed or unstayed for a period of more than ninety (90) days, then the other Party may by written notice terminate this Agreement in its entirety with immediate effect.

 

 

(i)           Licensee and Licensor each shall have the right to terminate this Agreement for default upon the other Party’s uncured failure to comply in any material respect with the terms and conditions of this Agreement.  At least sixty (60) days prior to any such termination for default, the Party seeking to so terminate shall give the other written notice of its intention to terminate this Agreement in accordance with the provisions of this Section 7.1(b)(i), which notice shall set forth the default(s) which form the basis for such termination.  If the defaulting Party fails to correct such default(s) within sixty (60) days after receipt of notification, or if the same cannot reasonably be corrected or remedied within sixty (60) days, or if the defaulting Party has not commenced curing such default(s) within such sixty (60) days and is not diligently pursuing completion of same, then such non-defaulting Party immediately may terminate this Agreement.

 

(ii)           This Section 7.1(b) shall not be an exclusive remedy and shall not be in lieu of any other remedies available to a Party hereto for any default hereunder on the part of the other Party.

 

 

7.2           Rights Upon Termination.  In the event of termination of this Agreement:

 

(a)           By Licensor under Section 7.1(b)(i) or Section 7.1(a), then the License shall automatically and immediately terminate.

 

(b)           By Licensee under Section 7.1(b)(i), then Licensee shall retain all of the rights under the License, subject to the Royalty payments set forth in Section 3.2.

 

7.3           Effect of Termination.  Upon any termination of this Agreement pursuant to this Article, and except as provided herein to the contrary, all rights and obligations of the Parties hereunder shall cease, except that the following rights and obligations shall survive:

 

(a)           Any rights to payment of Royalties arising or accrued prior to the effective date of termination;

 

(b)           Any cause of action or claim of either Party accrued or to accrue because of any breach or default by the other hereunder;

 

(c)           Subject to payment of the Royalty, Licensee shall have the right to sell its remaining inventory of Licensed Products which shall then be stored at Licensee's facilities or under issued orders from its customers and issued orders to its suppliers and contractors at the time of termination (and for such purpose the License, including without limitation the right hereunder to use any applicable trademark, shall continue).

 

(d)           The provisions of Articles 1, 6, 8 and 9 hereof; and

 

(e)           All other terms, provisions, representations, rights and obligations contained in this Agreement that by their sense and context are intended to survive until performance thereof by either or both Parties.

 

Figure 1 presents an illustration of a flat layout view of the Svelte helical stent having straight, diagonal connectors shown as cut before crimping onto a delivery balloon with the out-of-phase arrangement of the circumferential sets of strut members. This stent is formed of cobalt chromium alloy L605 and has the following dimensions:

 

Hybrid Stent with Helical Connectors	12/582,251	October 20, 2009

 

 

 

MEMORANDUM

To:	Svelte Medical Systems, Inc.

From:

Jonathan O’Brien, Ph.D. Andrew N. Weber

 

Re:	Executive Summary of Freedom to Operate Study of ‘Stent-on-a-Wire’ Product

Date:

October 26, 2009

 

 

 

Svelte Medical Systems, Inc. (“Svelte”) commissioned Honigman Miller Schwartz and Cohn LLP to investigate the state of the art for stent delivery systems that deploy an expandable stent within e vasculature of a body and to conduct an infringement analysis to determine whether Svelte’s proposed stent or stent delivery system infringes any third party patent references located during our investigation.

Svelte’s stent delivery system product includes a catheter, depicted in Figure 1, that deploys an expandable tent having a 2-dimensional pattern depicted in Figure 2.

Figure 1.  Catheter Delivery System.

 

 

 

 

Figure 2.  Expandable Stent.

A detailed description of Svelte’s stent delivery system product and our analysis is provided in a separate comprehensive opinion that includes a thorough discussion of the law, search results and relevant prosecution histories.  Briefly, our searches for U.S. patents and U.S. patent applications that are relevant to stent delivery systems and stents located over 650 patents and patent applications.  In particular, we reviewed the references listed below in Table 1 as well as those in the attached Appendix.

US 6,042,597

US 6,348,065

US 6,461,381

US 6,464,722

US 6,488,703

US 6,818,014

US 6,981,986

US 6,997,946

US 7,037,330

US 20090012598

US 5,470,313

US 5,843,116

US 6,007,543

US 6,027,517

US 6,077,273

US 6,306,162

US 6,371,962

US 6,432,129

US 6,468,230

US 6,835,189

US 6,918,920

US 20050171591

US 20080023346

 

 

Based on our current understanding of Svelte’s stent delivery system product, it is our opinion that none of the third party patents of which we are currently aware encumber the use, manufacture, and sale of this product.  It is also our opinion that Svelte would not be encumbered by third party patents issuing with the specific claims in their current form that are currently pending in the various applications discussed below.  Thus, it is our opinion that the use, manufacture, and sale of Svelte’s proposed stent delivery system and expandable stent will not infringe third party patents located in our reference search.  It is also our opinion that the use, manufacture, or sale of Svelte’s stent delivery system and expandable stent would not infringe the currently pending claims in any f the pending patent applications located in our reference search if those claims issued in their current form.

 

To the extent that Svelte is planning to make, have made, use, or sell its particular stent delivery system product, it is free to do so with the caveat that Svelte does not make improvements or other modifications to the stent delivery system product that are covered by valid third party patents.  Several entities, including Boston Scientific, Inc., have made or are making improvements to existing stent delivery systems including improvements to the stents themselves.  For example, some of these improvements include the placement of a mounting substrate between a balloon and a catheter shaft, the use of helical stent patterns, improvements to strut flexibilities in stents, the addition of retractable stent retaining sleeves, and the addition of core wires having different flexibilities along their lengths.  Several of these entities, have obtained patents and/or have rights to pending patent applications that cover various improvements.

 

Note that our opinion is based on our current understanding of Svelte’s stent delivery system and expandable stent, the references in our searches, and the claims as currently pending in the various patent applications described above.  This patent clearance study is limited to U.S. patents and pending U.S. applications that have published as of the date of this study.  Also note that it is possible that pertinent references, which may affect our opinion, were not identified by our reference search.  As with any patent clearance study, it should be borne in mind that each search is unavoidably dependent upon the completeness and accuracy of the databases searched.  Given the very large number of published patent documents, the references identified by separate searches using different search criteria are often not one hundred percent complementary.  It is unlikely that two different searchers would find the exact same patents even if they searched the same databases.  Furthermore, some relevant patents may not have been published at the time we conducted our searches.  Although we have endeavored to ensure the accuracy and reliability of this patent clearance study, we cannot guarantee that our searches identified every pertinent patent available as of the date of our search.  It is possible that pertinent references, which may affect our opinion, were not identified by our searchers.  Patent clearance studies are performed and opinions rendered on the results of such searches to reduce the risk of infringing a valid, issued patent.  It is impossible to remove the risk of patent infringement entirely.

 

Furthermore, it is our recommendation that Svelte continue to monitor the activities of other entities developing stents and stent delivery systems to ensure that latent infringement issues do not arise.

 

US4917666	US4950227	US5279560	US5290230	US5292321
US5320604	US5135487	US5328469	US5342305	US5342386
US5364354	US5324263	US5409495	US5417658	US5425711
US5470313	US5387225	US5549551	US5567203	US5571087
US5628755	US5474537	US5639274	US5645560	US5647847
US5632760	US5634928	US5733260	US5743876	US5749851
US5702364	US5720724	US5843116	US5843164	US5853408
US5800391	US5843092	US5957903	US5957930	US5871468
US5807327	US5951514	US6007543	US6027517	US5961536
US5944726	US6004291	US6113579	US6120523	US6042588
US5980533	US6077273	US6190332	US6190393	US6123712
US6068623	US6086556	US6264683	US6306162	US6200305
US6159219	US6174327	US6306144	US6371962	US6315790
US6159227	US6228110	US6355016	US6425908	US6375628
US6217667	US6251094	US6419685	US6432129	US6458138
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US6348060	US6409741	US6592570	US6520984	US6544222
US6402720	US6491711	US6676666	US6610069	US6623504
US6402778	US6589274	US6736839	US6692461	US6696121
US6475209	US6669670	US6830575	US6736841	US6761703
US6478814	US6579305	US6736827	US6835189	US6881216
US6663660	US6814744	US6954977	US6837869	US7048713
US6726714	US6936065	US7387640	US6872215	US7083577
US6802849	US7241273	US7025758	US7004963	US7465311
US6923787	US20010027337	US20020040232	US20020138127	US20020138128
US7226472	US20010032008	US20050215950	US7438720	US20030009129
US20010000350	US20020183780	US20020198521	US20020123794	US20030065352
US20020156519	US20030032941	US20030033000	US20020138081	US20030236563
US20030032921	US20030187494	US20030212410	US20030004535	US20040098082
US20030149465	US20040059277	US20040064130	US20030055378	US20050049671
US20040059276	US20040215141	US20040215317	US20030229307	US20050261722
US20040158256	US20050148866	US20050203563	US20040073250	US20070038283
US20050096724	US20050171591	US20060271093	US20050027247	US20070156087
US20050131512	US20060265046	US20070016240	US20050251195	US20080077223
US20060265040	US20060271090	US20070100280	US20070021817	US20080275390
US20070123805	US20070093781	US20070112370	US20070112408	US20090182408
US20060265041	US20080009933	US20080015675	US20090125094	US20090054875
US20070093780	US20080228171	US20080023346	US20080033525	US2009006987
US20070260177	US20090062773	US20080114294	US20080255507	US20090163879
US20080228138	US20090062835	US20080249465	US20090157050	US20090036967
US5295959	US5318535	US20090198317	US20020147491	US20030135256
US5357978	US5360401	US6203558	US6344045	US20040055926
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