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 ConMed CorporationLabelled 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 ConMed Linvatec with 21 510(k) clearances. The most recent is a 510(k) clearance dated Aug 8, 2011: Y-KNOT ALL-SUTURE ANCHOR MODEL HF13.
| Aug 8, 2011 | Y-KNOT ALL-SUTURE ANCHOR MODEL HF13K111779 · MBI | 510(k) clearances |
| Dec 21, 2010 | MATRYX INTERFERENCE SCREW (5.0-6.5MM)K102410 · HWC | 510(k) clearances |
| Nov 23, 2010 | CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICEK102339 · GAT | 510(k) clearances |
| Aug 26, 2010 | CROSSFT OC SUTURE ANCHOR MODE CFC-4502, CFC-5502, CFC-6502, CFC-4503, CFC-5503, CFC-6503K101100 · MAI | 510(k) clearances |
| Oct 19, 2009 | CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURESK092898 · MAI | 510(k) clearances |
| Jun 29, 2009 | CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYSK090560 · KCT | 510(k) clearances |
| Mar 27, 2009 | ZEN WIRELESS FOOTSWITCH (W1000), ZEN WIRELESS FOOTSWITCH ADAPTER (W1100)K083161 · HRX | 510(k) clearances |
| Sep 5, 2008 | CONMED LINVATEC MICROFRACTURE INSTRUMENT STERILIZATION TRAYK080531 · KCT | 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
