Medical Device Manufacturer · US , Tonawanda , NY

Ab Ardent - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1998

Total

Cleared

Denied

Ab Ardent has 13 FDA 510(k) cleared dental devices. Based in Tonawanda, US.

Historical record: 13 cleared submissions from 1998 to 2013.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Ab Ardent is one of 5154 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Ab Ardent — FDA 510(k) Products and Clearance History

13 devices

1-12 of 13

HIGH SILVER CONVENTIONAL

K020452 · EJJ

Dental · 85d

Cleared Aug 16, 2001

FUTURA TOPCAP NON GAMMA-2

K011801 · EJJ

Dental · 69d

Cleared Sep 17, 1999

FUTURA GLASS IONOMER SILVER REINFORCED

Ab Ardent - FDA 510(k) Cleared Devices

Ab Ardent — FDA 510(k) Products and Clearance History

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