Feeltech Co., Ltd.

Feeltech Co., Ltd. — FDA 510(k) Submissions

Feeltech Co., Ltd. has submitted 4 FDA 510(k) premarket notifications since 2018, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Surgical, Absorbable, Polydioxanone, Low Dead Space Piston Syringe . Use the specialty filter in the sidebar to narrow results.