Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Zimmer BiometLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Biomet Trauma with 11 510(k) clearances. The most recent is a 510(k) clearance dated May 3, 2011: MAC MALE ADAPTER.
| May 3, 2011 | MAC MALE ADAPTERK102843 · KTT | 510(k) clearances |
| May 21, 2010 | BIOMET FORERUNNER LOCKING PLATE SYSTEMK092528 · HRS | 510(k) clearances |
| Mar 19, 2010 | SMPLE PLATE AND SCREWSK093983 · HRS | 510(k) clearances |
| Mar 5, 2010 | OPTILOCK VL (VARIABLE ANGLE LOCKING) DISTAL RADIUS PLATING SYSTEMK093761 · HRS | 510(k) clearances |
| Aug 17, 2009 | BIOMET PHOENIX ANKLE NAIL AND ANKLE ARTHRODESIS NAILK091976 · HSB | 510(k) clearances |
| Aug 5, 2009 | OPTILOCK PERIARTICULAR PLATINGK092078 · HRS | 510(k) clearances |
| Feb 5, 2009 | BIODRIVE CANNULATED SCREW SYSTEMK082874 · HWC | 510(k) clearances |
| Jul 30, 2008 | LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONSK081244 · KTT | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
