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 & Nephew plcLabelled 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 Orthopaedics with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jun 3, 1999: OPERA CUPFLANGED ACETABULAR COMPONENTS.
| Jun 3, 1999 | OPERA CUPFLANGED ACETABULAR COMPONENTSK991538 · JDI | 510(k) clearances |
| Aug 14, 1997 | TITANIUM SPINAL ROD SYSTEMK970635 · KWQ | 510(k) clearances |
| Jul 16, 1997 | ZIRCONIA PROZYR CERAMIC 12/14 GLOBAL TAPER (GT) FEMORAL HEADSK971414 · LZO | 510(k) clearances |
| May 9, 1997 | TAYLOR SPATIAL FRAME EXTERNAL FIXATION SYSTEMK970748 · KTT | 510(k) clearances |
| Apr 16, 1997 | HEIDELBERG EXTERNAL FIXATORK970751 · JDW | 510(k) clearances |
| Apr 3, 1997 | COMPASS UNIVERSAL HINGEK970713 · JDW | 510(k) clearances |
| Feb 28, 1997 | HA GLOBAL TAPER (GT) TAPERED HIP STEMK970337 · MEH | 510(k) clearances |
| Feb 28, 1997 | GLOBAL TAPER SPECTRON HIP STEMSK970351 · 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
