Jewel Soft Tissue Reinforcement Device (102-6005)
Jul 2025
350d
Xiros Limited
1
Total
1
Cleared
0
Denied
Xiros Limited — FDA 510(k) Submissions
Xiros Limited has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Mesh, Surgical, Non-resorbable, Orthopedics, Reinforcement Of Ligament . Use the specialty filter in the sidebar to narrow results.
1 devices