Ushare Medical, Inc.

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

Ushare Medical, Inc. 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 Biopsy Needle, Hemostatic Wound Dressing Without Thrombin Or Other Biologics . Use the specialty filter in the sidebar to narrow results.