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Trice Medical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K241700
Tenex 2nd Generation System
November 18, 2024
K212556
mi-eye 3 needlescope with cannula, mi-tablet 3
September 15, 2021
K162475
mi-eye 2, mi-eye 2 monitor
September 16, 2016
K141119
CAMERA ENABLED PROBE
July 29, 2014