Ab Ardent
Ab Ardent holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2013.
Top product codes for Ab Ardent
Recent clearances by Ab Ardent
- K131753 — MERIDIAN
- K040465 — LATIT FLOW
- K022971 — MICROHYBRID 11
- K022972 — MICROFILL 13
- K022973 — ADHESIVE 14
- K022974 — MICROHYBRID 12
- K022975 — ETCHING 15
- K020452 — HIGH SILVER CONVENTIONAL
- K011801 — FUTURA TOPCAP NON GAMMA-2
- K991974 — FUTURA GLASS IONOMER SILVER REINFORCED
- K982456 — AMALCAP PLUS
- K982458 — VIVALLOY HR
- K982460 — VIVACAP HR
Data sourced from openFDA. This site is unofficial and independent of the FDA.