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Data / Medical devices / Bone Cement, Antibiotic / United States

FDA-registered makers of Bone Cement, Antibiotic in the United States: 12 establishments

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

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Device
Bone Cement, Antibiotic
Product code
MBB
Country
United States

Makers of Bone Cement, Antibiotic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Biomet, Inc.Warsaw, IN, United StatesContract manufacturer, Manufacturer7December 28, 2022000api.fda.gov
Depuy Orthopaedics, Inc.Warsaw, IN, United StatesManufacturer, Specification developer1May 14, 2008020api.fda.gov
Howmedica Osteonics CorpMahwah, NJ, United StatesSpecification developer1February 26, 2007020api.fda.gov
ArthroCare CorporationAustin, TX, United StatesSpecification developer0000api.fda.gov
C&A Tool Engineering, Inc. Auburn PlantAuburn, IN, United StatesContract manufacturer0000api.fda.gov
C+a Tool Engineering, Inc.Churubusco, IN, United StatesContract manufacturer0000api.fda.gov
Encore Medical, L.P.Austin, TX, United StatesManufacturer0000api.fda.gov
Freudenberg Medical, LLCCarpinteria, CA, United StatesContract manufacturer0000api.fda.gov
Millstone Medical Outsourcing LLCOlive Branch, MS, United StatesContract manufacturer0000api.fda.gov
Ortho Development Corp.Draper, UT, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Osteoremedies, LLCMemphis, TN, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Total Joint Orthopedics, Inc.Salt Lake City, UT, 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.