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Data / Medical devices / Components, Exercise / United States

FDA-registered makers of Components, Exercise in the United States: 39 establishments

39 establishments in the United States are registered with the FDA to make Components, Exercise (product code IOD). 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
Components, Exercise
Product code
IOD
Country
United States

Makers of Components, Exercise in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alimed, LLCDedham, MA, United StatesManufacturer, Specification developer0000api.fda.gov
ASP Global, LLCAustell, GA, United StatesSpecification developer0000api.fda.gov
Aspire Products, LLCSwansboro, NC, United StatesManufacturer0000api.fda.gov
Altimate Medical, Inc.Frankfort, IL, United StatesManufacturer0000api.fda.gov
Ashley Black Inc.Houston, TX, United StatesSpecification developer0000api.fda.gov
Barbaras Development, Inc.Thousand Oaks, CA, United StatesContract manufacturer0000api.fda.gov
Bird & Cronin, LLCEagan, MN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Boost Therapeutic Innovations, LLCGainesville, FL, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Breg, Inc.Carlsbad, CA, United StatesSpecification developer0000api.fda.gov
Core Products Intl., Inc.Osceola, WI, United StatesManufacturer0000api.fda.gov
Clinton Industries, IncYork, PA, United StatesManufacturer0000api.fda.gov
DepcoHauppauge, NY, United StatesManufacturer0000api.fda.gov
Djo, LLCCarlsbad, CA, United StatesSpecification developer0000api.fda.gov
E. Bac Si Imports LLCEllensburg, WA, United StatesSpecification developer0000api.fda.gov
Fabrication Ent., Inc.Elmsford, NY, United StatesManufacturer0000api.fda.gov
Fit For Life, LLCEmpire State, NY, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Flint Rehabilitation Devices, LLCIrvine, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Harvard MedtechLas Vegas, NV, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Implus Footcare LLCDurham, NC, United StatesSpecification developer0000api.fda.gov
Indica-Mcs LLCFowlerville, MI, United StatesContract manufacturer0000api.fda.gov
MASS Rehab Inc.Moraine, OH, United StatesContract manufacturer, Manufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
North Coast Medical, Inc.Morgan Hill, CA, United StatesManufacturer0000api.fda.gov
Optp LLCMinneapolis, MN, United StatesSpecification developer0000api.fda.gov
Orthomed, LLCWhittier, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
P.C.P. ChampionRipley, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Personal Medical Corp.Bothell, WA, United StatesManufacturer0000api.fda.gov
Plasticity NeurorehabilitationEvansville, IN, United StatesSpecification developer0000api.fda.gov
Professional Specialties Co., Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov
PTWorks, LLCPleasant Grove, UT, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Position Health, LLCLake Forest, IL, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Richardson Products, Inc.Frankfort, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Skil-Care Corp.New Rochelle, NY, United StatesContract manufacturer, Manufacturer0000api.fda.gov
The Hygenic Company, LLCAkron, OH, United StatesSpecification developer0000api.fda.gov
The Pettibon SystemChehalis, WA, United StatesManufacturer0000api.fda.gov
Theradapt Products Inc.Ludington, MI, United StatesManufacturer0000api.fda.gov
Therapeutic Dimensions Inc.Spokane, WA, United StatesSpecification developer0000api.fda.gov
Tiburon Medical EnterprisesSan Jacinto, CA, United StatesManufacturer0000api.fda.gov
Top Shelf Manufacturing, LLCTracy, CA, 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.