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 15, 2026, FDA's public records list Axya Medical with 19 510(k) clearances. The most recent is a 510(k) clearance dated Oct 11, 2007: AXYA, MODEL 3000 AXYZLOOP TITANIUM BONE ANCHOR.
| Oct 11, 2007 | AXYA, MODEL 3000 AXYZLOOP TITANIUM BONE ANCHORK070773 · MBI | 510(k) clearances |
| Jul 11, 2007 | AXYA SUTURE WELDING SYSTEM AND KITK070253 · GAT | 510(k) clearances |
| Dec 4, 2006 | TUFFLEX POLYESTER SUTUREK063194 · GAT | 510(k) clearances |
| Sep 1, 2006 | AXYAFLEX POLYESTER SUTUREK060165 · GAT | 510(k) clearances |
| Jul 5, 2006 | AXYALOOP NONABSORBABLE BONE ANCHORK060970 · JDR | 510(k) clearances |
| Oct 7, 2005 | AXYA MODEL 6500 AXYALOOP SELF-TAPPING BONE ANCHORK052491 · MBI | 510(k) clearances |
| Aug 5, 2005 | MODEL 3000 AXYALOOP BIO-ABSORBABLE BONE ANCHORK051983 · MAI | 510(k) clearances |
| Jun 9, 2005 | AXYA, MODEL 6500 AXYALOOP BIO-ABSORBABLE BONE ANCHORK051250 · 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
