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Data / Medical devices / Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment / United States

FDA-registered makers of Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment in the United States: 34 establishments

34 establishments in the United States are registered with the FDA to make Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment (product code KIJ). 7 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
Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment
Product code
KIJ
Country
United States

Makers of Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Smith & Nephew Inc.Oklahoma City, OK, United StatesManufacturer2May 7, 1982000api.fda.gov
Acumed LLCHillsboro, OR, United StatesManufacturer1May 7, 1996000api.fda.gov
OsteomedAddison, TX, United StatesComplaint file establishment, Manufacturer, Specification developer1November 7, 1994000api.fda.gov
R & D Batteries, Inc.Burnsville, MN, United StatesManufacturer1April 5, 1994000api.fda.gov
Smith & Nephew Inc.Andover, MA, United StatesSpecification developer1May 7, 1982000api.fda.gov
Smith & Nephew Inc.Mansfield, MA, United StatesManufacturer1May 7, 1982000api.fda.gov
Stryker InstrumentsPortage, MI, United StatesComplaint file establishment, Specification developer1September 4, 1997000api.fda.gov
ARCH Medical Solutions - WarsawWarsaw, IN, United StatesContract manufacturer0000api.fda.gov
B & J Medical LLCKendallville, IN, United StatesContract manufacturer0000api.fda.gov
BioDynamikLake Forest, CA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Depuy Orthopaedics, Inc.Warsaw, IN, United StatesSpecification developer0000api.fda.gov
DePuy Mitek, Inc.Raynham, MA, United StatesSpecification developer0000api.fda.gov
Insurgical, Inc.Austin, TX, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
KLS-Martin L.P.Jacksonville, FL, United StatesSpecification developer0000api.fda.gov
LaVezzi Precision, IncBloomingdale, IL, United StatesContract manufacturer0000api.fda.gov
Mainstream Medical DevicesAustin, TX, United StatesComplaint file establishment, Contract manufacturer, Manufacturer0000api.fda.gov
Microaire Surgical Instruments LLCCharlottesville, VA, United StatesManufacturer0000api.fda.gov
Micropulse IncColumbia City, IN, United StatesContract manufacturer0000api.fda.gov
Millstone Medical Outsourcing LLC.Fall River, MA, United StatesContract manufacturer0000api.fda.gov
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN, United StatesContract manufacturer0000api.fda.gov
Norwood Medical LLCDayton, OH, United StatesContract manufacturer0000api.fda.gov
Onyx Medical LLCMemphis, TN, United StatesContract manufacturer0000api.fda.gov
Orthopediatrics, CorpWarsaw, IN, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Packaging Compliance Medical, LLCKentwood, MI, United StatesContract manufacturer0000api.fda.gov
Paragon Medical, Inc.Pierceton, IN, United StatesContract manufacturer0000api.fda.gov
Peleton SurgicalScottsdale, AZ, United StatesSpecification developer0000api.fda.gov
Precision Medical TechnologiesWarsaw, IN, United StatesContract manufacturer0000api.fda.gov
Paragon Medical Inc.Castleton, IN, United StatesContract manufacturer0000api.fda.gov
Paragon Medical Inc.Smithfield, UT, United StatesContract manufacturer0000api.fda.gov
Shalby Advanced Technologies, Inc.El Dorado Hills, CA, United StatesManufacturer0000api.fda.gov
Spineology Inc.Saint Paul, MN, United StatesManufacturer0000api.fda.gov
Stryker Manufacturing KalamazooPortage, MI, United StatesContract manufacturer0000api.fda.gov
Universal Punch Corp.Santa Ana, CA, United StatesContract manufacturer0000api.fda.gov
VorzeigenConnersville, IN, United StatesContract manufacturer0000api.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.