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

FDA-registered makers of Suture, Nonabsorbable, Synthetic, Polyamide in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Suture, Nonabsorbable, Synthetic, Polyamide (product code GAR). 12 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device
Suture, Nonabsorbable, Synthetic, Polyamide
Product code
GAR
Country
United States

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

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
S. Jackson, Inc.Alexandria, VA, United StatesManufacturer4December 17, 1993100api.fda.gov
CovidienNorth Haven, CT, United StatesManufacturer, Specification developer2July 13, 1998020api.fda.gov
Riverpoint Medical LLCPortland, OR, United StatesComplaint file establishment, Manufacturer, Specification developer2October 28, 2015010api.fda.gov
Tas Medical, Inc.Windermere, FL, United StatesComplaint file establishment, Specification developer2June 3, 2026010api.fda.gov
Antarma LLCNew York, NY, United StatesComplaint file establishment, Specification developer1March 31, 2022000api.fda.gov
Aros Surgical Instruments CorporationNorth Wales, PA, United StatesSpecification developer1October 14, 2004000api.fda.gov
Alcon Research, LLCSinking Spring, PA, United StatesManufacturer1December 17, 1993000api.fda.gov
Demetech Corp.Miami Lakes, FL, United StatesManufacturer1June 18, 2003000api.fda.gov
Nashville Surgical InstrumentsSpringfield, TN, United StatesSpecification developer1July 15, 2008000api.fda.gov
SYNOVIS MICRO COMPANIES ALLIANCE, INC. (a subsidiary of Baxter International Inc.)Birmingham, AL, United StatesSpecification developer1October 28, 2015000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer1July 7, 1998010api.fda.gov
Visionary Medical Supplies, Inc.Madison, WI, United StatesManufacturer1February 8, 2000000api.fda.gov
Ethicon, Inc.Somerville, NJ, United StatesManufacturer0000api.fda.gov
Ethicon, Inc.Raritan, NJ, United StatesManufacturer0000api.fda.gov
Ethicon, LLCGuaynabo, PR, United StatesManufacturer0000api.fda.gov
Ethicon, LLC.San Lorenzo, PR, United StatesManufacturer, Manufacturer for export0000api.fda.gov
Ethicon LLCManati, PR, United StatesManufacturer0000api.fda.gov
Kollsut International IncNorth Miami Beach, FL, United StatesManufacturer0000api.fda.gov
Performance Fibers OEM LLCMansfield, MA, United StatesContract manufacturer0000api.fda.gov
R.K. ManufacturingDanbury, CT, United StatesContract manufacturer0000api.fda.gov
Sharp Fluidics, Inc.El Granada, CA, United StatesSpecification developer0000api.fda.gov
Sirius Engineering LLCSan Carlos, CA, United StatesContract manufacturer0000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler0000api.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.