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Data / Medical devices / Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery / United States

FDA-registered makers of Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery in the United States: 11 establishments

11 establishments in the United States are registered with the FDA to make Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery (product code OXH). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery
Product code
OXH
Country
United States

Makers of Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Integra LifeSciences Braintree Inc.Braintree, MA, United StatesManufacturer1June 7, 2017000api.fda.gov
Acell, Inc.Columbia, MD, United StatesManufacturer0000api.fda.gov
Bard Shannon LimitedHumacao, PR, United StatesContract manufacturer0000api.fda.gov
Boston Scientific Corp., Marina Bay Cust. Fulfillment CenterQuincy, MA, United StatesManufacturer0000api.fda.gov
Boston Scientific CorporationRoswell, GA, United StatesManufacturer, Specification developer0000api.fda.gov
Cook Biotech, Inc.West Lafayette, IN, United StatesManufacturer0000api.fda.gov
Davol Inc., Sub. C.R. Bard, Inc.Warwick, RI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
DSM Biomedical, Inc.Exton, PA, United StatesManufacturer0000api.fda.gov
Lifecell CorpBranchburg, NJ, United StatesManufacturer0000api.fda.gov
Lifecell Corp.Branchburg, NJ, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
RTI Surgical, Inc. (dba RTI Biologics, Inc.)Alachua, FL, 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.