Medical Device Manufacturer · US , Lancaster , PA

Dentalez Group - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1988
13
Total
13
Cleared
0
Denied

Dentalez Group has 13 FDA 510(k) cleared dental devices. Based in Lancaster, US.

Historical record: 13 cleared submissions from 1988 to 2003.

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) Regulatory Record - Dentalez Group
13 devices
1-12 of 13
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