Xiros, Ltd.

Xiros, Ltd. — FDA 510(k) Submissions

Xiros, Ltd. has submitted 9 FDA 510(k) premarket notifications since 2015, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mesh, Surgical, Polymeric, Fastener, Fixation, Nondegradable, Soft Tissue, Suture, Nonabsorbable, Synthetic, Polyethylene, Washer, Bolt Nut, Pin, Fixation, Smooth . Use the specialty filter in the sidebar to narrow results.