Sprintray, Inc.

Sprintray, Inc. — FDA 510(k) Submissions

Sprintray, Inc. has submitted 8 FDA 510(k) premarket notifications since 2021, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Resin, Denture, Relining, Repairing, Rebasing, Material, Tooth Shade, Resin, Crown And Bridge, Temporary, Resin, Mouthguard, Prescription . Use the specialty filter in the sidebar to narrow results.