Medical Device Manufacturer · CN , Suzhou

Endoclot Plus Co., Ltd.

3 submissions · 3 cleared · Since 2017
3
Total
3
Cleared
0
Denied

Endoclot Plus Co., Ltd. — FDA 510(k) Submissions

Endoclot Plus Co., Ltd. has submitted 3 FDA 510(k) premarket notifications since 2017, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Hemostatic Device For Endoscopic Gastrointestinal Use, Submucosal Injection Agent . Use the specialty filter in the sidebar to narrow results.

3 devices
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All3 General & Plastic Surgery 2 Gastroenterology & Urology 1