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Data / Medical devices / Suture, Nonabsorbable, Synthetic, Polypropylene / United States

FDA-registered makers of Suture, Nonabsorbable, Synthetic, Polypropylene in the United States: 24 establishments

24 establishments in the United States are registered with the FDA to make Suture, Nonabsorbable, Synthetic, Polypropylene (product code GAW). 18 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.

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Device
Suture, Nonabsorbable, Synthetic, Polypropylene
Product code
GAW
Country
United States

Makers of Suture, Nonabsorbable, Synthetic, Polypropylene in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
CovidienNorth Haven, CT, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer4June 1, 2005020api.fda.gov
Ethicon, Inc.Raritan, NJ, United StatesManufacturer, Specification developer3March 27, 2026000api.fda.gov
Nobles Medical Technologies II, Inc.Fountain Valley, CA, United StatesSpecification developer3April 19, 2012000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler3March 19, 2020000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer3March 19, 2020000api.fda.gov
Ethicon, Inc.Somerville, NJ, United StatesManufacturer2December 6, 2013010api.fda.gov
Ethicon, LLCGuaynabo, PR, United StatesManufacturer2March 27, 2026000api.fda.gov
Ethicon, LLC.San Lorenzo, PR, United StatesManufacturer2December 6, 2013010api.fda.gov
HeartStitch, INC.Fountain Valley, CA, United StatesContract manufacturer, Manufacturer2April 19, 2012000api.fda.gov
Lsi Solutions Inc.Victor, NY, United StatesManufacturer2September 15, 2016000api.fda.gov
Cypris Medical, Inc.Evanston, IL, United StatesSpecification developer1January 12, 2024000api.fda.gov
Demetech Corp.Miami Lakes, FL, United StatesManufacturer1May 16, 2005000api.fda.gov
Ethicon LLCManati, PR, United StatesManufacturer1December 6, 2013000api.fda.gov
Kmi Imi Group / Dba: Innovative Med, Inc.Irvine, CA, United StatesManufacturer1March 4, 2005000api.fda.gov
Mesh Suture, IncChicago, IL, United StatesComplaint file establishment, Specification developer1September 2, 2022000api.fda.gov
Riverpoint Medical LLCPortland, OR, United StatesComplaint file establishment, Manufacturer, Specification developer1June 23, 2000000api.fda.gov
Visionary Medical Supplies, Inc.Madison, WI, United StatesManufacturer1April 17, 2007000api.fda.gov
W. L. Gore & Associates, Inc.Elkton, MD, United StatesManufacturer0100api.fda.gov
Alcon Research, LLCSinking Spring, PA, United StatesManufacturer0000api.fda.gov
Kollsut International IncNorth Miami Beach, FL, United StatesManufacturer0000api.fda.gov
Norwood Medical LLCDayton, OH, United StatesContract manufacturer0000api.fda.gov
Performance Fibers OEM LLCMansfield, MA, United StatesContract manufacturer0000api.fda.gov
SYNOVIS MICRO COMPANIES ALLIANCE, INC. (a subsidiary of Baxter International Inc.)Birmingham, AL, United StatesSpecification developer0000api.fda.gov
Vaupell Midwest Molding and ToolingConstantine, MI, United StatesContract manufacturer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.