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 Arthocare Corporation with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jan 19, 2016: MultiFIX S Ultra Knotless Fixation System.
| Jan 19, 2016 | MultiFIX S Ultra Knotless Fixation SystemK153669 · MBI | 510(k) clearances |
| Jul 29, 2013 | MULTIFIX S KNOTLESS FIXATION DEVICEK131182 · MBI | 510(k) clearances |
| Dec 11, 2012 | AMBIENT TURBOFLASH 90 IFSK120791 · GEI | 510(k) clearances |
| Nov 7, 2012 | SMARTSTITCH PERFECTPASSER SYSTEMK123268 · GAT | 510(k) clearances |
| Jul 12, 2012 | SMARTSTITCH M-CONNECTOR ULTRA SMARTSTITCH SUTURE DEVICE HANDLE SMARTSTITCH SUTURE DEVICE HANDLEK121306 · GAT | 510(k) clearances |
| Dec 13, 2001 | ENDOFLIPK013334 · MBI | 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
