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Data / Medical devices / Orthosis, Foot Drop / United States

FDA-registered makers of Orthosis, Foot Drop in the United States: 24 establishments

24 establishments in the United States are registered with the FDA to make Orthosis, Foot Drop (product code OHI). 0 have 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
Orthosis, Foot Drop
Product code
OHI
Country
United States

Makers of Orthosis, Foot Drop in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alimed, LLCDedham, MA, United StatesManufacturer, Specification developer0000api.fda.gov
Aspen Business Solutions LLCNorth Ogden, UT, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Aspen Medical Products, LLCIrvine, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Axiobionics, LLC, Center for NeuroprostheticsAnn Arbor, MI, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Becker Orthopedic Appliance Co.Troy, MI, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Biosculptor CorporationHialeah, FL, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Brace AlignSoddy Daisy, TN, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Braceability, Inc.Cedar Falls, IA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
COYOTE O&P, IncBoise, ID, United StatesManufacturer0000api.fda.gov
Doctor In The HouseBlue Bell, PA, United StatesManufacturer0000api.fda.gov
Footscientific, Inc.Draper, UT, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Flint Rehabilitation Devices, LLCIrvine, CA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Hersco-Orthotic Labs CorpLong Island City, NY, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Insightful ProductsFalmouth, ME, United StatesManufacturer0000api.fda.gov
La Pointique International Ltd.Seattle, WA, United StatesSpecification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Oppo Medical, Inc.Seattle, WA, United StatesSpecification developer0000api.fda.gov
Orthomerica Products, Inc.Orlando, FL, United StatesManufacturer0000api.fda.gov
Pine Tree Orthopedic Lab, Inc.Livermore Falls, ME, United StatesContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Professional Products, Inc.Defuniak Spgs, FL, United StatesManufacturer0000api.fda.gov
ProtostheticsFargo, ND, United StatesContract manufacturer0000api.fda.gov
Relief MedicalPhoenix, AZ, United StatesSpecification developer0000api.fda.gov
RX Orthotic IncArcadia, CA, United StatesContract manufacturer0000api.fda.gov
Saebo, Inc.Charlotte, NC, United StatesManufacturer0000api.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.