Paragon Implant Mfg., LLC

Paragon Implant Mfg., LLC — FDA 510(k) Submissions

Paragon Implant Mfg., LLC has submitted 4 FDA 510(k) premarket notifications since 2025, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Endosseous, Root-form, Sterilization Wrap Containers, Trays, Cassettes & Other Accessories . Use the specialty filter in the sidebar to narrow results.