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Data / Medical devices / Orthosis, Truncal/Orthosis, Limb / United States

FDA-registered makers of Orthosis, Truncal/Orthosis, Limb in the United States: 34 establishments

34 establishments in the United States are registered with the FDA to make Orthosis, Truncal/Orthosis, Limb (product code MRI). 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
Orthosis, Truncal/Orthosis, Limb
Product code
MRI
Country
United States

Makers of Orthosis, Truncal/Orthosis, Limb in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
3M CompanySaint Paul, MN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Becker Orthopedic Appliance Co.Troy, MI, United StatesManufacturer0000api.fda.gov
Benik Corp.Silverdale, WA, United StatesManufacturer0000api.fda.gov
Boston Brace International, IncorporatedStoughton, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Braceability, Inc.Cedar Falls, IA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Breg, Inc.Carlsbad, CA, United StatesSpecification developer0000api.fda.gov
Core Products Intl., Inc.Osceola, WI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Core Products International IncChetek, WI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Doctor In The HouseBlue Bell, PA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
E. Bac Si Imports LLCEllensburg, WA, United StatesSpecification developer0000api.fda.gov
Green Sun MedicalSan Rafael, CA, United StatesManufacturer0000api.fda.gov
Joerns HealthcareCharlotte, NC, United StatesSpecification developer0000api.fda.gov
Joerns HealthcareArlington, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
M&M Pure Air Systems LLCLewes, DE, United StatesManufacturer0000api.fda.gov
Medi-Dyne Healthcare Products, Inc.Colleyville, TX, United StatesSpecification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Motion TherapeuticsFolsom, CA, United StatesManufacturer0000api.fda.gov
Ontel Products CorporationFairfield, NJ, United StatesSpecification developer0000api.fda.gov
Optec Usa, Inc.Lawrenceville, GA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Orthocor Medical Inc.Blaine, MN, United StatesManufacturer0000api.fda.gov
Pelvic Binder, Inc.Cumby, TX, United StatesManufacturer0000api.fda.gov
PMT Corp.Chanhassen, MN, United StatesManufacturer, Remanufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Portland Garment FactoryPortland, OR, United StatesContract manufacturer0000api.fda.gov
Pro-Tech InternationalRaynham, MA, United StatesManufacturer0000api.fda.gov
Spinal Technology, LLCWest Yarmouth, MA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Spio Inc.Burien, WA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Surestep, LLCSouth Bend, IN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Spinal Systems, LLCLouisville, KY, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Symbiont Logistics, LLCPhoenix, AZ, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Tarry Medical Products, Inc.Danbury, CT, United StatesManufacturer0000api.fda.gov
Theratogs, Inc.Telluride, CO, United StatesManufacturer0000api.fda.gov
Tiburon Medical EnterprisesSan Jacinto, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Trulife, Inc.Bellingham, WA, United StatesManufacturer0000api.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.