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 EndoscopyLabelled 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 Endoscopy, Inc. with 18 510(k) clearances. The most recent is a 510(k) clearance dated Feb 3, 2011: OSTEORAPTOR CURVED 2.3 SUTURE ANCHORS.
| Feb 3, 2011 | OSTEORAPTOR CURVED 2.3 SUTURE ANCHORSK103309 · MAI | 510(k) clearances |
| Dec 13, 2010 | BIORAPTOR CURVED 2.3 PK SUTURE ANCHORSK102660 · MBI | 510(k) clearances |
| Dec 17, 2009 | SMITH & NEPHEW KNOTLESS INSTABILITY ANCHORK093428 · MBI | 510(k) clearances |
| Jan 30, 2009 | SMITH & NEPHEW BIOSURE PK INTERFERENCE SCREWK083635 · MBI | 510(k) clearances |
| Jan 30, 2009 | SMITH & NEPHEW PEEK INTERFERENCE SCREWK083226 · MBI | 510(k) clearances |
| Oct 21, 2008 | ULTRASLIDE ACROMIOCLAVICULAR AND SYNDESMOTIC REPAIR DEVICEK082095 · HTN | 510(k) clearances |
| Apr 20, 2005 | SMITH & NEPHEW INTELIJET FLUID MANAGEMENT SYSTEMSK050580 · HRX | 510(k) clearances |
| Jan 12, 2000 | BIORCI SCREWK992396 · HWC | 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
