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.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Osteobiologics, Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Oct 25, 2005: OCT (OSTEOCHONDRAL TRANSPLANT) COMPREHENSIVE SYSTEM.
| Oct 25, 2005 | OCT (OSTEOCHONDRAL TRANSPLANT) COMPREHENSIVE SYSTEMK051656 · HRX | 510(k) clearances |
| Jun 17, 2005 | POLYGRAFT BGS; BONE GRAFT SUBSTITUTEK041382 · JDK | 510(k) clearances |
| Jan 7, 2005 | TRUGRAFT BGS SYRINGE, MODEL 600-041K043172 · FMF | 510(k) clearances |
| Dec 17, 2004 | POLYGRAFT BGS; BONE GRAFT SUBSTITUTEK040047 · MQV | 510(k) clearances |
| Aug 16, 2004 | POLYGRAFT TCP GRANULES, CUBES, BLOCKS, PLUGS, WEDGES, MODELS 600-023-XX, 600-025-XX, 600-026-XX, 600-022-XX, 600-027-XXK033707 · MQV | 510(k) clearances |
| Oct 2, 2003 | IMMIX PLASTIFILMK032673 · FTL | 510(k) clearances |
| Jul 17, 2003 | POLYGRAFT BONE GRAFT SUBSTITUTEK030288 · MQV | 510(k) clearances |
| Mar 14, 2003 | IMMIX THIN FILM, MODELS: PSS-004-S, PSS-004-SP, PSS-004-M, PSS-004-MP, PSS-004-L, PSS-004-LPK024199 · FTL | 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
