Grindguard, Inc.

Grindguard, Inc. — FDA 510(k) Submissions

Grindguard, Inc. has submitted 2 FDA 510(k) premarket notifications since 2025, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mouthguard, Prescription, Impression Material For Fabrication Of Patient-matched Mouthguards, Over-the-counter . Use the specialty filter in the sidebar to narrow results.