Austenal, Inc.
Austenal, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2001.
Top product codes for Austenal, Inc.
Recent clearances by Austenal, Inc.
- K011674 — DC - CRISTAL
- K001799 — DC-TELL
- K001815 — DC ZIRKON
- K001798 — DC TITAN
- K970522 — MYERSON'S ECONOMY DENTURE BASE MATERIAL
- K970205 — VITALLIUM 2000 ALLOY; VITALLIUM 2000 PLUS ALLOY; COBALT CHROME CASTING ALLOY
- K955509 — MIDAS GOLD ELECTROFORMING SYSTEM
- K954810 — MYERSON IR DENTURE BASE
- K933468 — MYERSON'S PERMASOFT SOFT RELINE MATERIAL
- K924526 — DENTURE PLASTIC TEETH
Data sourced from openFDA. This site is unofficial and independent of the FDA.