Theramicro - FDA 510(k) Cleared Devices
Recent clearances: TeKBrace Solo Soft Tissue Reinforcement Device, TekBrace Solo Soft Tissue Reinforcement Device, TeKBrace Knotless Anchor
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Theramicro Orthopedic ✕
4 devices
Cleared
Aug 18, 2026
TeKBrace Solo Soft Tissue Reinforcement Device
Orthopedic
18d
Cleared
Jun 09, 2026
TekBrace Solo Soft Tissue Reinforcement Device
Orthopedic
25d
Cleared
Mar 06, 2026
TeKBrace Knotless Anchor
Orthopedic
113d
Cleared
May 30, 2025
TekBrace Solo Soft Tissue Reinforcement Device
Orthopedic
56d