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Data / Medical devices / Monitor, Orthotic/Prosthetic / United States

FDA-registered makers of Monitor, Orthotic/Prosthetic in the United States: 8 establishments

8 establishments in the United States are registered with the FDA to make Monitor, Orthotic/Prosthetic (product code NHF). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Monitor, Orthotic/Prosthetic
Product code
NHF
Country
United States

Makers of Monitor, Orthotic/Prosthetic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Boston Brace International, IncorporatedStoughton, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Click MedicalSteamboat Springs, CO, United StatesManufacturer0000api.fda.gov
Comfort Products, Inc.Croydon, PA, United StatesManufacturer0000api.fda.gov
Innovative Neurotronics Inc.Reno, NV, United StatesManufacturer0000api.fda.gov
Levy & RappelSaddle Brook, NJ, United StatesManufacturer0000api.fda.gov
Opos1Waterloo, IA, United StatesSpecification developer0000api.fda.gov
Spinal Technology, LLCWest Yarmouth, MA, United StatesSpecification developer0000api.fda.gov
Spinal Systems, LLCLouisville, KY, United StatesSpecification developer0000api.fda.gov

Updated November 3, 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.