Nvision Biomedical Technologies, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Nvision Biomedical Technologies, Inc. has 22 FDA 510(k) cleared orthopedic devices. Based in San Antonio, US.
Latest FDA clearance: Nov 2025. Active since 2019.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Nvision Biomedical Technologies, Inc.
22 devices
Cleared
Nov 18, 2025
ToeJack MIS Bunion System
Orthopedic
54d
Cleared
Sep 19, 2025
Impact PEEK Union Nail System
Orthopedic
28d
Cleared
Apr 02, 2025
SnapHammer Hammertoe Correction System
Orthopedic
33d
Cleared
Sep 17, 2024
3D Printed PEEK Interbody System
Orthopedic
231d
Cleared
Feb 16, 2024
SnapHammer Hammertoe Correction System
Orthopedic
274d
Cleared
Oct 06, 2023
EARP Nerve Cuff Electrode
Neurology
192d
Cleared
Jul 05, 2023
Integral Titanium Cervical Interbody
Orthopedic
362d
Cleared
Dec 01, 2022
Trigon™ HA Stand-Alone Wedge Fixation System
Orthopedic
44d
Cleared
Apr 28, 2022
EARP Interbody System
Orthopedic
262d
Cleared
Feb 23, 2022
Trigon HA Wedge Fixation System
Orthopedic
30d
Cleared
Nov 24, 2021
The Radian MIS Bunion System
Orthopedic
180d
Cleared
Nov 19, 2021
Vector® Hammertoe Correction System
Orthopedic
30d