Nvision Biomedical Technologies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
36
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253423ToeJack MIS Bunion SystemNovember 18, 2025
K252657Impact PEEK Union Nail SystemSeptember 19, 2025
K250646Impact PEEK Union Nail SystemJune 11, 2025
K250613SnapHammer Hammertoe Correction SystemApril 2, 2025
K242896Caliber Intramedullary Fixation SystemFebruary 5, 2025
K243231Trigon PEEK HA WedgesNovember 8, 2024
K2402503D Printed PEEK Interbody SystemSeptember 17, 2024
K231453SnapHammer Hammertoe Correction SystemFebruary 16, 2024
K234116Trigon Trigon HA Stand-Alone Wedge Fixation SystemJanuary 26, 2024
K230853EARP Nerve Cuff ElectrodeOctober 6, 2023
K222015Integral Titanium Cervical InterbodyJuly 5, 2023
K223226Trigon™ HA Stand-Alone Wedge Fixation SystemDecember 1, 2022
K212477EARP Interbody SystemApril 28, 2022
K220197Trigon HA Wedge Fixation SystemFebruary 23, 2022
K211650The Radian MIS Bunion SystemNovember 24, 2021
K213421Vector® Hammertoe Correction SystemNovember 19, 2021
K210424Quantum Anterior Cervical PlateOctober 22, 2021
K203445Trigon HA Stand-Alone Wedge Fixation SystemDecember 21, 2020
K202657Javelin Tailor's Bunion Fixation SystemDecember 14, 2020
K200428Multi-Drive Interference Screw SystemNovember 10, 2020