Medical Device Manufacturer · US , Wilmington , DE

Reazeal Corp

1 submissions · 1 cleared · Since 2023

Total

Cleared

Denied

Reazeal Corp — FDA 510(k) Submissions

Reazeal Corp has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mouthguard, Over-the-counter . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

Mouth Guard (ATG0603R)

K231865 · OBR Mouthguard, Over-the-counter · Dental

Nov 2023 133d

Reazeal Corp

Reazeal Corp — FDA 510(k) Submissions

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