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Data / Medical devices / Component, Traction, Invasive / United States

FDA-registered makers of Component, Traction, Invasive in the United States: 25 establishments

25 establishments in the United States are registered with the FDA to make Component, Traction, Invasive (product code JEC). 12 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.

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Device
Component, Traction, Invasive
Product code
JEC
Country
United States

Makers of Component, Traction, Invasive in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Biomet, Inc.Warsaw, IN, United StatesManufacturer7June 16, 1994000api.fda.gov
Synthes (USA) Products LLCWest Chester, PA, United StatesComplaint file establishment, Specification developer4August 24, 2007000api.fda.gov
Acumed LLCHillsboro, OR, United StatesManufacturer3February 19, 1997010api.fda.gov
Hand Biomechanics Lab, Inc.Sacramento, CA, United StatesManufacturer3October 22, 2018010api.fda.gov
Depuy Orthopaedics, Inc.Warsaw, IN, United StatesSpecification developer2January 11, 1990000api.fda.gov
Depuy Spine, Inc.Raynham, MA, United StatesSpecification developer2December 15, 1999000api.fda.gov
G-5 Florida LLCJax, FL, United StatesManufacturer2March 2, 2020010api.fda.gov
Orthofix Us LLCLewisville, TX, United StatesRepackager or relabeler, Specification developer2April 4, 1995000api.fda.gov
Virak Orthopedics LLCMadison, NJ, United StatesRepackager or relabeler, Specification developer2October 10, 2019000api.fda.gov
JMG Machine, Inc.La Mirada, CA, United StatesContract manufacturer, Manufacturer1February 22, 1994000api.fda.gov
KLS-Martin L.P.Jacksonville, FL, United StatesSpecification developer1August 25, 2004000api.fda.gov
Medline ReNewalRedmond, OR, United StatesReprocessor1December 28, 2016000api.fda.gov
Advanced Concept Innovations LLCLakeland, FL, United StatesContract manufacturer0000api.fda.gov
Arthrex, Inc.Naples, FL, United StatesSpecification developer0000api.fda.gov
HPC MedxHanover, PA, United StatesContract manufacturer0000api.fda.gov
Micropulse IncColumbia City, IN, United StatesContract manufacturer0000api.fda.gov
NUTEK Orthopaedics, IncFort Lauderdale, FL, United StatesSpecification developer0000api.fda.gov
Onyx Medical LLCMemphis, TN, United StatesContract manufacturer0000api.fda.gov
Orchid UniqueBridgeport, MI, United StatesContract manufacturer0000api.fda.gov
Symmetry Medical Manufacturing IncClaypool, IN, United StatesContract manufacturer0000api.fda.gov
Symmetry Medical Manufacturing Inc.Warsaw, IN, United StatesContract manufacturer0000api.fda.gov
Stryker Sustainability SolutionsTempe, AZ, United StatesSpecification developer0000api.fda.gov
Stryker Sustainability Solutions PhoenixPhoenix, AZ, United StatesReprocessor0000api.fda.gov
Wright Medical Technology, Inc.Arlington, TN, United StatesManufacturer0000api.fda.gov
Wright Medical Technology, Inc.Arlington, TN, United StatesComplaint file establishment, Specification developer0000api.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.