Incore Co., Ltd.

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

Incore Co., Ltd. has submitted 6 FDA 510(k) premarket notifications since 2022, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Hemostatic Metal Clip For The Gi Tract, Laparoscopic Single Port Access Device, Snare, Flexible, Endoscopic Injection Needle, Gastroenterology-urology . Use the specialty filter in the sidebar to narrow results.