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 Johnson & Johnson. FDA records under its name, each linked to the record. See the Johnson & Johnson group view.
As of Nov 15, 2026, FDA's public records list Johnson & Johnson Orthopaedics with 22 510(k) clearances. The most recent is a 510(k) clearance dated Dec 6, 1994: PFC MODULAR TOTAL KNEE SYSTEM, POROUS COATED SACRI.
| Dec 6, 1994 | PFC MODULAR TOTAL KNEE SYSTEM, POROUS COATED SACRIK931466 · JWH | 510(k) clearances |
| Oct 6, 1994 | P.F.C. 2 TOTAL HIP SYSTEM POROUS COATED MODULAR FEMORAL COMPONENTK935452 · LZO | 510(k) clearances |
| Sep 29, 1994 | ULTIMA UNIPOLAR MODULAR HEADK940190 · KWL | 510(k) clearances |
| Sep 28, 1994 | P.F.C. CERAMIC HIP HEADK933275 · LZO | 510(k) clearances |
| Sep 20, 1994 | ORTHOSORB(TM) ABSORBABLE CEMENT RESTRICTORK932595 · LZN | 510(k) clearances |
| Jun 9, 1994 | P.F.C. BIPOLAR HIP SYSTEMK931655 · KWY | 510(k) clearances |
| Jun 6, 1994 | UNIVERSAL INSET PATELLAK933867 · JWH | 510(k) clearances |
| Jun 3, 1994 | P.F.C. TOTAL KNEE SYSTEM OVAL PATELLAK935262 · JWH | 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
