Etex Corp.
Etex Corp. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2010.
Top product codes for Etex Corp.
Recent clearances by Etex Corp.
- K100883 — CARRIGEN
- K101557 — GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGEN
- K093447 — CARRIGEN
- K091729 — ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
- K091607 — ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
- K090855 — EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE
- K090310 — EQUIVABONE
- K090242 — GAMMA-BSM, BETA-BSM
- K080329 — CAP PLUS, EQUIVABONE, CAP/DBM
- K063050 — CAP PLUS
- K072636 — A-BSM BONE SUBSTITUTE MATERIAL
- K072355 — OSSIFUSE BONE SUBSTITUTE MATERIAL
- K062630 — OSSIPRO BONE SUBSTITUTE MATERIAL
- K033138 — CAP3 BONE SUBSTITUTE MATERIAL
- K032307 — CAP BONE SUBSTITUTE MATERIAL
- K983009 — BSM- BONE SUBSTITUTE MATERIAL
- K962548 — BSM BONE SUBSTITUTE MATERIAL KIT
- K935696 — ETEX HA HIP REPLACEMENT SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.