Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FinlandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of ConMedLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Linvatec Biomaterials with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 25, 2005: MATRYX INTERFERENCE SCREW.
| Aug 25, 2005 | MATRYX INTERFERENCE SCREWK052080 · HWC | 510(k) clearances |
| Nov 19, 2004 | DUET SUTURE ANCHOR, MODELS BXS4216, BXS4216H; IMPACT SUTURE ANCHOR, MODELS BXS4218, BXS4218HK042966 · MAI | 510(k) clearances |
| Oct 8, 2004 | BIOSORB FX AND BIOSORB PDX 1.5 AND 2.0 SCREWSK042517 · JEY | 510(k) clearances |
| Sep 16, 2004 | SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020K042295 · HWC | 510(k) clearances |
| Jun 10, 2004 | MODIFICATION TO SMARTPINK041288 · HTY | 510(k) clearances |
| May 7, 2004 | OSTEO ACL SCREW MODEL;237020T, 237025T, 237030T, 238020T, 238025T, 238030T, 239020T, 239025T, 239030T, 231020T, 231025T,K032894 · HWC | 510(k) clearances |
| Apr 16, 2004 | CANNULATED NUGEN FX SCREW FULLY THREADED, CANNULATED NUGEN FX SCREW PARTIALLY THREADEDK032447 · HWC | 510(k) clearances |
| Jul 25, 2003 | 2.4 SMARTNAIL, MODELS 532416, 532425, 532435, 532445K031981 · MAI | 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
