Viz. Ai, Inc.

Viz. Ai, Inc. holds 11 FDA 510(k) medical device clearances, first cleared 2018, most recent 2025.

Top product codes for Viz. Ai, Inc.

Recent clearances by Viz. Ai, Inc.

K250354 — Viz Subdural+, Viz SUBDURAL PLUSCode QIH·2025-06-10
K232363 — Viz HDS, Viz Volume Plus, Viz ICH+Code QIH·2024-02-05
DEN230003 — Viz HCMCode QXO·2023-08-03
K223443 — Viz AAACode QFM·2023-03-17
K223042 — Viz LVO ContaCTCode QAS·2022-10-21
K221100 — Viz RV/LVCode QIH·2022-08-29
K220439 — Viz SDHCode QAS·2022-07-25
K213319 — Viz ANEURYSM, Viz ANXCode QFM·2022-02-18
K210209 — Viz ICHCode QAS·2021-03-23
K193658 — Viz ICHCode QAS·2020-03-18
K180161 — Viz CTPCode LLZ·2018-04-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.