Skip to the page

Data / Medical devices / Suture, Absorbable, Synthetic / United States

FDA-registered makers of Suture, Absorbable, Synthetic in the United States: 8 establishments

8 establishments in the United States are registered with the FDA to make Suture, Absorbable, Synthetic (product code GAN). 5 have a 510(k) clearance or PMA approval on file and 1 has 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.

Device
Suture, Absorbable, Synthetic
Product code
GAN
Country
United States

Makers of Suture, Absorbable, Synthetic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ethicon, Inc.San Angelo, TX, United StatesManufacturer2December 18, 1996000api.fda.gov
Ethicon, Inc.Somerville, NJ, United StatesManufacturer2December 18, 1996000api.fda.gov
Ethicon, Inc.Raritan, NJ, United StatesSpecification developer2December 18, 1996010api.fda.gov
Ethicon, LLCGuaynabo, PR, United StatesManufacturer2December 18, 1996000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler1July 5, 1990000api.fda.gov
Kollsut International IncNorth Miami Beach, FL, United StatesManufacturer0000api.fda.gov
Microaire Surgical Instruments LLCCharlottesville, VA, United StatesManufacturer0000api.fda.gov
Performance Fibers OEM LLCMansfield, MA, 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.