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Data / Medical devices / Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile / United States

FDA-registered makers of Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile in the United States: 19 establishments

19 establishments in the United States are registered with the FDA to make Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile (product code GAQ). 13 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, Steel, Monofilament And Multifilament, Sterile
Product code
GAQ
Country
United States

Makers of Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ethicon, Inc.Somerville, NJ, United StatesManufacturer3November 1, 2017010api.fda.gov
Ethicon, Inc.Raritan, NJ, United StatesManufacturer, Specification developer3November 1, 2017000api.fda.gov
Ethicon, LLCGuaynabo, PR, United StatesManufacturer2November 1, 2017000api.fda.gov
Ethicon, LLC.San Lorenzo, PR, United StatesManufacturer2November 1, 2017020api.fda.gov
Synthes (USA) Products LLCWest Chester, PA, United StatesSpecification developer2May 27, 2005000api.fda.gov
Conextions IncSalt Lake City, UT, United StatesComplaint file establishment, Manufacturer1April 22, 2022000api.fda.gov
CovidienNorth Haven, CT, United StatesSpecification developer1February 27, 1996000api.fda.gov
Demetech Corp.Miami Lakes, FL, United StatesManufacturer1September 25, 2014000api.fda.gov
Ethicon LLCManati, PR, United StatesManufacturer1January 9, 1995000api.fda.gov
Kollsut International IncNorth Miami Beach, FL, United StatesManufacturer1February 19, 2020000api.fda.gov
Riverpoint Medical LLCPortland, OR, United StatesComplaint file establishment, Specification developer1March 28, 2003000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler1July 26, 1994000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer1July 26, 1994020api.fda.gov
Alto Development Corp.Farmingdale, NJ, United StatesSpecification developer0000api.fda.gov
Fort Wayne Metals Research Products, LLCFort Wayne, IN, United StatesContract manufacturer0000api.fda.gov
Jabil Inc. (Brandywine)W Chester, PA, United StatesContract manufacturer0000api.fda.gov
Jabil Inc. (Monument)Monument, CO, United StatesContract manufacturer0000api.fda.gov
Performance Fibers OEM LLCMansfield, MA, United StatesContract manufacturer0000api.fda.gov
Pioneer Surgical Technology, Inc.Marquette, 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.