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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Anulex Technologies with 12 510(k) clearances. The most recent is a 510(k) clearance dated Nov 9, 2012: MICRO/MINI N-PK(F) BONE ANCHOR.
| Date | Record | Source |
|---|---|---|
| Nov 9, 2012 | MICRO/MINI N-PK(F) BONE ANCHORK121354 · MBI | 510(k) clearances |
| Nov 9, 2012 | MICRO/MINI N-PK(H) BONE ANCHORK121356 · MBI | 510(k) clearances |
| Feb 23, 2012 | FIXATE TISSUE BANDK113805 · GZB | 510(k) clearances |
| Dec 16, 2011 | FIXATE TISSUE BANDK113400 · GZB | 510(k) clearances |
| Oct 27, 2011 | FIXATE TISSUE BANDK112849 · GZB | 510(k) clearances |
| Sep 8, 2011 | FIXATE TISSUE BANDK111462 · GZB | 510(k) clearances |
| Mar 17, 2010 | VERSACLOSE, MODEL VC-200-01K100572 · GAT | 510(k) clearances |
| Jun 12, 2009 | XCLOSE TISSUE REPAIR SYSTEM, MODEL XC-200-01K091432 · GAT | 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
