Erchonia Medical, Inc.

Erchonia Medical, Inc. — FDA 510(k) Submissions

Erchonia Medical, Inc. has submitted 10 FDA 510(k) premarket notifications since 2004, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powered Light Based Laser Non-thermal Instrument With Non-heating Effect For Adjunctive Use In Pain Therapy, Fat Reducing Low Level Laser, Powered Laser Surgical Instrument, Device, Iontophoresis, Other Uses, Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis . Use the specialty filter in the sidebar to narrow results.