Nvision Biomedical Technologies is one of 16117 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nvision Biomedical Technologies - FDA 510(k) Cleared Devices
Recent clearances: EnHAnce PEEK Bunion System, Impact PEEK Union Nail System, Caliber Intramedullary Fixation System
5
Total
5
Cleared
0
Denied
Nvision Biomedical Technologies has 5 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Latest FDA clearance: Sep 2026. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Nvision Biomedical Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nvision Biomedical Technologies
5 devices
Cleared
Sep 18, 2026
EnHAnce PEEK Bunion System
Orthopedic
88d
Cleared
Jun 11, 2025
Impact PEEK Union Nail System
Orthopedic
99d
Cleared
Feb 05, 2025
Caliber Intramedullary Fixation System
Orthopedic
135d
Cleared
Nov 08, 2024
Trigon PEEK HA Wedges
Orthopedic
30d
Cleared
Jan 26, 2024
Trigon Trigon HA Stand-Alone Wedge Fixation System
Orthopedic
30d