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Data / Medical devices / Prosthesis, Ankle, Uncemented, Non-Constrained / United States

FDA-registered makers of Prosthesis, Ankle, Uncemented, Non-Constrained in the United States: 14 establishments

14 establishments in the United States are registered with the FDA to make Prosthesis, Ankle, Uncemented, Non-Constrained (product code NTG). 2 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Device
Prosthesis, Ankle, Uncemented, Non-Constrained
Product code
NTG
Country
United States

Makers of Prosthesis, Ankle, Uncemented, Non-Constrained in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
DT Medtech LLCMcMinnville, TN, United StatesSpecification developer0120api.fda.gov
Encore Medical, L.P.Austin, TX, United StatesComplaint file establishment, Specification developer0100api.fda.gov
Arthrosurface, Inc.W Bridgewater, MA, United StatesManufacturer for export0000api.fda.gov
Avalign Delivery Systems DivisionGreenwood, IN, United StatesContract manufacturer0000api.fda.gov
Avalign Instruments & ImplantsFort Wayne, IN, United StatesContract manufacturer0000api.fda.gov
Biomet, Inc.Warsaw, IN, United StatesManufacturer0000api.fda.gov
Exactech, Inc.Gainesville, FL, United StatesManufacturer for export0010api.fda.gov
Isomedix Operations Inc.Northborough, MA, United StatesManufacturer for export0000api.fda.gov
Isomedix Operations, Inc.Libertyville, IL, United StatesContract sterilizer, Manufacturer for export0000api.fda.gov
Medical Modeling - A 3D Systems CompanyLittleton, CO, United StatesContract manufacturer0000api.fda.gov
Medin Technologies, Inc.Totowa, NJ, United StatesContract manufacturer0000api.fda.gov
Millstone Medical Outsourcing LLC.Fall River, MA, United StatesContract manufacturer0000api.fda.gov
Orchid UniqueBridgeport, MI, United StatesContract manufacturer0000api.fda.gov
Zimmer, Inc.Warsaw, IN, United StatesManufacturer for export0000api.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.