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Data / Medical devices / Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained / United States

FDA-registered makers of Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained in the United States: 18 establishments

18 establishments in the United States are registered with the FDA to make Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained (product code JWJ). 6 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
Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained
Product code
JWJ
Country
United States

Makers of Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Smith & Nephew, Inc.Memphis, TN, United StatesManufacturer3May 30, 2024000api.fda.gov
Biomet, Inc.Warsaw, IN, United StatesManufacturer2July 29, 2008000api.fda.gov
Arthrosurface, Inc.W Bridgewater, MA, United StatesManufacturer1October 15, 2020000api.fda.gov
Extremity Medical, LLCParsippany, NJ, United StatesSpecification developer1March 4, 2020000api.fda.gov
Janco, Inc.Rollinsford, NH, United StatesContract manufacturer, Repackager or relabeler1March 4, 2020000api.fda.gov
Skeletal Dynamics, IncMiami, FL, United StatesComplaint file establishment, Specification developer1July 3, 2024000api.fda.gov
ARCH Medical Solutions - WarsawWarsaw, IN, United StatesContract manufacturer0000api.fda.gov
Instru-Med TechnologiesWarsaw, IN, United StatesContract manufacturer0000api.fda.gov
Micro Precision SwissSanta Ana, CA, United StatesContract manufacturer0000api.fda.gov
Millstone Medical Outsourcing LLC.Fall River, MA, United StatesContract manufacturer0000api.fda.gov
Metal Craft Machine & Engineering, Inc.Elk River, MN, United StatesContract manufacturer0000api.fda.gov
Onyx Medical LLCMemphis, TN, United StatesContract manufacturer0000api.fda.gov
Orchid Orthopedics-ChelseaChelsea, MI, United StatesContract manufacturer0000api.fda.gov
Orchid UniqueBridgeport, MI, United StatesContract manufacturer0000api.fda.gov
Pro-Tech Design & MFG., Inc.Santa Fe Springs, CA, United StatesContract manufacturer0000api.fda.gov
Quality Tech Services, LLCBloomington, MN, United StatesContract manufacturer0000api.fda.gov
Riverside Machine & Engineering, Inc.Eau Claire, WI, United StatesContract manufacturer0000api.fda.gov
RMS Co.Minneapolis, MN, 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.