Kono Seisakusho Co., Ltd.

Kono Seisakusho Co., Ltd. — FDA 510(k) Submissions

Kono Seisakusho Co., Ltd. has submitted 2 FDA 510(k) premarket notifications since 2020, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Nonabsorbable, Synthetic, Polyamide, Clamp, Vascular . Use the specialty filter in the sidebar to narrow results.