Drawing for FLUOROPASSIV

USPTO serial 79189100

FLUOROPASSIV

Reviewed by CopyMark Law Group

Reg. 5135131Status 709
Filing date
Status date
Registration date
Feb 7, 2017
Examiner
VAGHANI, MAYUR C
Law office
PUBLICATION AND ISSUE SECTION

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This page summarizes the public USPTO record for this serial number, including owners, goods and services, and prosecution history.

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Owner

Attorney of record

The USPTO lists this attorney as the applicant's representative for correspondence on this application.

JEFFREY H. GREGER

JEFFREY H. GREGER ROBERTSMLOTKOWSKISAFRANCOLE&CALDERONPC7918 JONES BRANCH DRIVE, SUITE 500MCLEAN, VA 22102UNITED STATES

Goods and services

ClassDescriptionStatusFirst use
010Surgical apparatus and instruments; medical apparatus and instruments for use in cardiovascular procedures; prosthetic vascular grafts; prosthetic endovascular grafts; stents, vascular prostheses; vascular prostheses with flared outflow; vascular prostheses with customisable outflow; prosthetic vascular woven grafts; prosthetic endovascular knitted grafts; expanded polytetrafluoroethylene (ePTFE) vascular grafts; surgical implants comprising prosthetic materials; suture materials; patches for repair and reconstruction of internal tissue, namely, cardiovascular patches, pericardial patches, and carotid patches, namely, surgical mesh comprised primarily of prosthetic materials; implantable medical systems, namely, cardiac valves for surgical prostheses, stents, prosthetic vascular grafts, vascular prostheses, prosthetic vascular grafts, prosthetic endovascular grafts, and catheters; implantable medical devices, namely, implants consisting of prosthetic materials, synthetic vascular prostheses, prosthetic vascular grafts, and synthetic heart valve conduits; prosthetic vascular grafts; prosthetic endovascular grafts; surgical graft materials, namely, prosthetic vascular grafts, and vascular prostheses for the treatment of aneurysmal or occlusive arterial disease; medical devices for use in endovascular procedures, namely, medical devices for use in treating cardiovascular disease; synthetic thoracic stents; synthetic thoracic stent grafts; synthetic stent grafts; synthetic stent graft systems comprised of synthetic stent grafts, stent delivery systems, and stent graft delivery systems; stent graft systems comprising more than one component comprised of synthetic stent grafts, stent delivery systems, and stent graft delivery systems; stent graft systems comprising components of more than one stent graft comprised of synthetic stent grafts, stent delivery systems, and stent graft delivery systems; stent graft systems comprising components of more than one type of stent graft comprised of synthetic stent grafts, stent delivery systems, and stent graft delivery systems; thoracic stent graft systems comprised of synthetic stent grafts, stent delivery systems, and stent graft delivery systems; prosthetic systemic vascular grafts; prosthetic vascular straight grafts; prosthetic vascular abdominal grafts; prosthetic vascular thoracic grafts; prosthetic vascular branched grafts; prosthetic vascular pre-curved grafts; prosthetic vascular aortic arch grafts; prosthetic vascular branched arch grafts; delivery systems for synthetic stent graft systems comprised of medical instruments for intraluminal emplacement of stents or of synthetic stent grafts, namely, stent or synthetic stent graft delivery systems; aneurysm repair systems comprised of catheter delivered stent grafts, medical instruments for intraluminal emplacement of stents or stent systems or of synthetic stent grafts, namely, stent delivery systems or stent graft delivery systems or synthetic stent graft delivery systems; medical devices, namely, aneurysm repair devices; cardiac valves for surgical prostheses; cardiac valve replacement systems, namely, prosthetic cardiac valves; heart valves, namely, prosthetic heart valves; heart valve conduits, namely, catheters for implanting heart valves; cardiac patches, namely, cardiovascular patches, pericardial patches, and carotid patches, namely, surgical mesh comprised primarily of prosthetic materials; vascular patches, namely, cardiovascular patches, pericardial patches, and carotid patches, surgical mesh comprised primarily of prosthetic materials; thin wall cardiovascular patches, namely, surgical mesh comprised primarily of prosthetic materials; thin wall carotid patches, namely, surgical mesh comprised primarily of prosthetic materials; fluoropolymer cardiovascular patches, namely, surgical mesh comprised primarily of prosthetic materials; fluoropolymer carotid patches, namely, surgical mesh comprised primarily of prosthetic materials; knitted cardiovascular patches, namely, surgical mesh comprised primarily of prosthetic materials; knitted carotid patches, namely, surgical mesh comprised primarily of prosthetic materials; gelatin sealed cardiovascular patches, namely, surgical mesh comprised primarily of prosthetic materials; gelatin sealed carotid patches, namely, surgical mesh comprised primarily of prosthetic materials; parts and fittings for all of the aforementioned goodsSECTION 71 - CANCELLED

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CopyMark links this record to cited §2(d) serials, the owner's other marks, Nice classes, similar mark names, and recently changed USPTO applications.

Prosecution history

DateCodeEventWhat it means
May 21, 2024INNTTOTAL INVALIDATION PROCESSED BY THE IB
Apr 30, 2024INTSTOTAL INVALIDATION OF REG EXT PROTECTION SENT TO IB
Apr 30, 2024INPCINVALIDATION PROCESSED
Apr 18, 2024INTRTOTAL INVALIDATION OF REG EXT PROTECTION CREATED
Aug 18, 2023C71TCANCELLED SECTION 71
Feb 7, 2022REM3COURTESY REMINDER - SEC. 71 (6-YR) E-MAILED
Jun 24, 2017FINOFINAL DECISION TRANSACTION PROCESSED BY IB
Jun 3, 2017FICSFINAL DISPOSITION NOTICE SENT TO IB
Jun 3, 2017FIMPFINAL DISPOSITION PROCESSED
May 7, 2017FICRFINAL DISPOSITION NOTICE CREATED, TO BE SENT TO IB
Feb 7, 2017R.PRREGISTERED-PRINCIPAL REGISTERYour trademark is registered on the Principal Register — the strongest form of federal trademark protection. You may use the ® symbol for the covered goods and services. Maintenance filings (Section 8 and renewals) are required to keep the registration alive.
Nov 22, 2016NPUBOFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
Nov 22, 2016PUBOPUBLISHED FOR OPPOSITIONYour mark was published in the USPTO Official Gazette for a 30-day opposition window. During that period, third parties who believe they would be harmed can file an opposition. If no opposition is filed, prosecution usually continues toward registration or a Notice of Allowance.
Nov 2, 2016NONPNOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
Oct 17, 2016PREVLAW OFFICE PUBLICATION REVIEW COMPLETED
Oct 13, 2016CNSAAPPROVED FOR PUB - PRINCIPAL REGISTER
Sep 22, 2016TEMETEAS/EMAIL CORRESPONDENCE ENTERED
Sep 22, 2016CRFACORRESPONDENCE RECEIVED IN LAW OFFICE
Sep 17, 2016ALIEASSIGNED TO LIE
Sep 8, 2016TCCATEAS CHANGE OF CORRESPONDENCE RECEIVED
Sep 8, 2016TROATEAS RESPONSE TO OFFICE ACTION RECEIVEDThis event means the applicant filed a response to a USPTO Office Action — typically arguments, amendments, or evidence addressing the examiner's objections. The USPTO will review the response and either allow the mark to proceed or issue another action.
Aug 5, 2016RFNTREFUSAL PROCESSED BY IB
Jul 20, 2016RFCSNON-FINAL ACTION MAILED - REFUSAL SENT TO IB
Jul 20, 2016RFRRREFUSAL PROCESSED BY MPU
Jul 20, 2016RFCRNON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW
Jul 19, 2016CNRTNON-FINAL ACTION WRITTENA non-final Office Action means the USPTO examining attorney has raised at least one issue with your trademark application but has not made a final decision. You usually have three months to respond with arguments, amendments, or evidence. Missing the deadline can abandon the application.
Jul 19, 2016MAFRAPPLICATION FILING RECEIPT MAILED
Jul 15, 2016DOCKASSIGNED TO EXAMINER
Jul 15, 2016NWOSNEW APPLICATION OFFICE SUPPLIED DATA ENTERED
Jul 14, 2016REPRSN ASSIGNED FOR SECT 66A APPL FROM IB

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