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 Smith & NephewLabelled 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 15, 2026, FDA's public records list Smith & Nephew Richards, Inc. with 87 510(k) clearances. The most recent is a 510(k) clearance dated May 8, 1997: EMPOWER ANTERIOR DIRECT SCREWS.
| May 8, 1997 | EMPOWER ANTERIOR DIRECT SCREWSK965224 · KWP | 510(k) clearances |
| Jan 27, 1997 | GLOBAL TAPER TAPERED HIP SYSTEM, GT SPECTRONK963509 · LPH | 510(k) clearances |
| Jan 24, 1997 | FINN ROD TO ROD CONNECTORK960444 · KWP | 510(k) clearances |
| Dec 27, 1996 | TRIMAX NAIL SYSTEMK964163 · HSB | 510(k) clearances |
| Dec 5, 1996 | GENESIS II ZIRCONIUM FEMORAL COMPONENT/PROFIX ZIRCONIUM FEMORAL COMPONENTK962557 · JWH | 510(k) clearances |
| Nov 27, 1996 | REVISION HIP SYSTEMK963486 · JDI | 510(k) clearances |
| Sep 17, 1996 | REFLECTION ACETABULAR REINFORCEMENT RINGSK962541 · JDJ | 510(k) clearances |
| Aug 19, 1996 | ILIZAROV EXTERNAL FIXATION SYSTEMK962808 · 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
