Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Orthopaedic Biosystems, Ltd. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Apr 3, 2000: OBL 2.0 MM MINI TAC ANCHOR, MODEL 10-1629-01.
| Apr 3, 2000 | OBL 2.0 MM MINI TAC ANCHOR, MODEL 10-1629-01K000797 · JDR | 510(k) clearances |
| Mar 4, 1999 | POLYMER OBL SB ANCHOR / SUTURE COMBINATIONK982996 · JDR | 510(k) clearances |
| Dec 16, 1998 | POLYMER THREADED ANCHORK983169 · MBI | 510(k) clearances |
| Nov 20, 1998 | POLYMER THREADED ANCHOR / SUTURE COMBINATIONK982963 · JDI | 510(k) clearances |
| Feb 6, 1998 | PEBA ANCHOR/SUTURE COMBINATIONK972326 · MBI | 510(k) clearances |
| Nov 15, 1996 | CANCELLOUS SCREW WASHERK963420 · HTN | 510(k) clearances |
| Nov 13, 1996 | GUIDE WIRES FOR CANNULATED SCREWSK963432 · LXT | 510(k) clearances |
| Nov 6, 1996 | THREADED FIXATION PINK963433 · JDW | 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
