Medical Device Manufacturer · US , New York , NY

Coltene/Whaledent AG - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 2005

Total

Cleared

Denied

Coltene/Whaledent AG has 16 FDA 510(k) cleared dental devices. Based in New York, US.

Historical record: 16 cleared submissions from 2005 to 2019.

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

FDA 510(k) cleared devices by Coltene/Whaledent AG

16 devices

1-12 of 16

BRILLIANT EverGlow Flow

PARAPOST PARACORE AUTOMIX 5ML

K052820 · EBF

Dental · 97d

Coltene/Whaledent AG - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Coltene/Whaledent AG

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