Viz. Ai, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250354Viz Subdural+, Viz SUBDURAL PLUSJune 10, 2025
K232363Viz HDS, Viz Volume Plus, Viz ICH+February 5, 2024
DEN230003Viz HCMAugust 3, 2023
K223443Viz AAAMarch 17, 2023
K223042Viz LVO ContaCTOctober 21, 2022
K221100Viz RV/LVAugust 29, 2022
K220439Viz SDHJuly 25, 2022
K213319Viz ANEURYSM, Viz ANXFebruary 18, 2022
K210209Viz ICHMarch 23, 2021
K193658Viz ICHMarch 18, 2020
K180161Viz CTPApril 20, 2018