Medical Device Manufacturer · US , Pocomoke City , MD

Dentimedic

1 submissions · 1 cleared · Since 1986

Total

Cleared

Denied

Dentimedic — FDA 510(k) Submissions

Dentimedic has submitted 1 FDA 510(k) premarket notifications since 1986, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Zinc Oxide Eugenol . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

DENTIMEDIC DENTAL EMERGENCY KIT

K861681 · EMB Zinc Oxide Eugenol · Dental

Sep 1986 145d

Dentimedic

Dentimedic — FDA 510(k) Submissions

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