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Data / Medical devices / Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) / United States

FDA-registered makers of Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) (product code JDL). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)
Product code
JDL
Country
United States

Makers of Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Biomet, Inc.Warsaw, IN, United StatesManufacturer2July 1, 1992000api.fda.gov
Howmedica Osteonics CorpMahwah, NJ, United StatesManufacturer2September 20, 1994020api.fda.gov
Microport Orthopedics Inc.Arlington, TN, United StatesManufacturer, Manufacturer for export2July 11, 2007000api.fda.gov
Depuy Orthopaedics, Inc.Warsaw, IN, United StatesSpecification developer1May 18, 1994000api.fda.gov
Depuy Orthopaedics, Inc.Raynham, MA, United StatesManufacturer1May 18, 1994000api.fda.gov
Shalby Advanced Technologies, Inc.El Dorado Hills, CA, United StatesManufacturer1July 21, 1993000api.fda.gov
Aps Materials, Inc.Dayton, OH, United StatesContract manufacturer0000api.fda.gov
ARCH - QuakertownQuakertown, PA, United StatesContract manufacturer0000api.fda.gov
ARCH Medical Solutions - SeabrookSeabrook, NH, United StatesContract manufacturer0000api.fda.gov
Avalign Instruments & ImplantsFort Wayne, IN, United StatesContract manufacturer0000api.fda.gov
Donson Machine CompanyAlsip, IL, United StatesContract manufacturer0000api.fda.gov
Himed, LLCOld Bethpage, NY, United StatesContract manufacturer0000api.fda.gov
Isomedix Operations Inc.Spartanburg, SC, United StatesContract sterilizer, Manufacturer for export0000api.fda.gov
Ken-Mar Machine MFG CorpPaterson, NJ, United StatesContract manufacturer0000api.fda.gov
LH Medical CorporationFort Wayne, IN, United StatesContract manufacturer0000api.fda.gov
Lincotek MedicalBartlett, TN, United StatesContract manufacturer0000api.fda.gov
Single Source Medical LLCChurubusco, IN, 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
Vaupell Midwest Molding and ToolingConstantine, MI, United StatesContract manufacturer0000api.fda.gov
Zimmer, Inc.Warsaw, IN, 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.