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Data / Medical devices / Joint, Hip, External Brace / United States

FDA-registered makers of Joint, Hip, External Brace in the United States: 26 establishments

26 establishments in the United States are registered with the FDA to make Joint, Hip, External Brace (product code ITS). 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
Joint, Hip, External Brace
Product code
ITS
Country
United States

Makers of Joint, Hip, External Brace in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Air A Med, LLCFort Myers, FL, United StatesSpecification developer0000api.fda.gov
Alpha Medical L.L.C.Rock Hill, SC, United StatesManufacturer0000api.fda.gov
Becker Orthopedic Appliance Co.Troy, MI, United StatesManufacturer0000api.fda.gov
Brace AlignSoddy Daisy, TN, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Breg, Inc.Carlsbad, CA, United StatesSpecification developer0000api.fda.gov
Djo, LLCCarlsbad, CA, United StatesContract manufacturer, Specification developer0000api.fda.gov
Fillauer, LLCChattanooga, TN, United StatesManufacturer0000api.fda.gov
Greenwood Marketing LLCBrandenburg, KY, United StatesComplaint file establishment, Contract manufacturer, Manufacturer0000api.fda.gov
Icarus Medical LLCCharlottesville, VA, United StatesManufacturer0000api.fda.gov
Incrediwear Holdings, Inc.Chico, CA, United StatesManufacturer, Specification developer0000api.fda.gov
La Pointique International Ltd.Seattle, WA, United StatesSpecification developer0000api.fda.gov
Manamed LLCDenton, TX, United StatesSpecification developer0000api.fda.gov
MD OrthopaedicsWayland, IA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Oppo Medical, Inc.Seattle, WA, United StatesSpecification developer0000api.fda.gov
Optec Usa, Inc.Lawrenceville, GA, United StatesManufacturer0000api.fda.gov
Orthomerica Products, Inc.Orlando, FL, United StatesContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Preferred Industries, Inc.Fort Lauderdale, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Professional Products, Inc.Defuniak Spgs, FL, United StatesManufacturer0000api.fda.gov
Precision Medical ProductsRocklin, CA, United StatesSpecification developer0000api.fda.gov
Secured Ortho Manufacturing Of America, LLCDeer Park, NY, United StatesManufacturer, Specification developer0000api.fda.gov
ST&G Usa Corporation / ChoiBrea, CA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Tiburon Medical EnterprisesSan Jacinto, CA, United StatesManufacturer0000api.fda.gov
Top Shelf Manufacturing, LLCTracy, CA, United StatesManufacturer0000api.fda.gov
Trend Medical, LLCBethlehem, PA, United StatesSpecification developer0000api.fda.gov
Unite Medical, LLCLithia Springs, GA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
pfs med, incSpringfield, OR, United StatesManufacturer, Remanufacturer0000api.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.