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Data / Medical devices / Suture, Nonabsorbable, Silk / United States

FDA-registered makers of Suture, Nonabsorbable, Silk in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Suture, Nonabsorbable, Silk (product code GAP). 8 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

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Device
Suture, Nonabsorbable, Silk
Product code
GAP
Country
United States

Makers of Suture, Nonabsorbable, Silk in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler4November 23, 2016000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer3November 23, 2016010api.fda.gov
Arrow International, LLC (subsidiary of Teleflex Incorporated)Wyomissing, PA, United StatesSpecification developer1July 17, 2007000api.fda.gov
CovidienNorth Haven, CT, United StatesManufacturer1May 11, 1998030api.fda.gov
Demetech Corp.Miami Lakes, FL, United StatesManufacturer1November 25, 2002000api.fda.gov
Kollsut International IncNorth Miami Beach, FL, United StatesManufacturer1June 9, 2008000api.fda.gov
Riverpoint Medical LLCPortland, OR, United StatesComplaint file establishment, Manufacturer, Specification developer1June 23, 2000000api.fda.gov
Visionary Medical Supplies, Inc.Madison, WI, United StatesManufacturer1February 8, 2000000api.fda.gov
Arthrex, Inc.Naples, FL, United StatesSpecification developer0000api.fda.gov
Alcon Research, LLCSinking Spring, PA, United StatesManufacturer, Manufacturer for export0000api.fda.gov
Arthrex Logistic CenterFort Myers, FL, United StatesManufacturer0000api.fda.gov
Arthrex Manufacturing Inc.Pendleton, SC, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
Arthrex, Inc.Ave Maria, FL, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
DSM Biomedical, Inc.Exton, PA, United StatesContract manufacturer0000api.fda.gov
Ethicon, Inc.Somerville, NJ, United StatesManufacturer0030api.fda.gov
Ethicon, Inc.Raritan, NJ, United StatesManufacturer0000api.fda.gov
Ethicon, LLCGuaynabo, PR, United StatesManufacturer0000api.fda.gov
Ethicon, LLC.San Lorenzo, PR, United StatesManufacturer0000api.fda.gov
Ethicon LLCManati, PR, United StatesManufacturer0000api.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

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.