Medical device makerLabelled 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 Implant Technology, Inc. with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jan 11, 1995: HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESIS.
| Jan 11, 1995 | HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESISK921525 · LPH | 510(k) clearances |
| May 28, 1992 | LSF HA COATED FEMORAL HIPK915617 · MEH | 510(k) clearances |
| Mar 25, 1992 | LSF TOTAL HIP SYSTEM - MULLER-TYPE ACETABULAR CUPK920021 · JDI | 510(k) clearances |
| Nov 7, 1991 | LSF DIAGNOSTIC RELATED GROUP CEMENTED HIPK913616 · JDI | 510(k) clearances |
| Aug 9, 1990 | LSF CEMENTED FEMORAL HIPK902727 · JDI | 510(k) clearances |
| May 22, 1990 | LSF(TM) TOTAL HIP SYSTEMK901460 · JDI | 510(k) clearances |
| May 2, 1989 | IMPLANT TECHNOLOGY BONE CEMENT EXTRACTORK891472 · LZV | 510(k) clearances |
| Dec 9, 1988 | MODIFIED LSF TOTAL HIP SYSTEMK884432 · JDI | 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
