Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Viz. Ai, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories4
Latest FDA decision2025-06-10
TypeNumberDevice NameCodeDateActions
510(k) K250354 Viz Subdural+, Viz SUBDURAL PLUSQIH2025-06-10 View
510(k) K232363 Viz HDS, Viz Volume Plus, Viz ICH+QIH2024-02-05 View
510(k) K223443 Viz AAAQFM2023-03-17 View
510(k) K223042 Viz LVO ContaCTQAS2022-10-21 View
510(k) K221100 Viz RV/LVQIH2022-08-29 View
510(k) K220439 Viz SDHQAS2022-07-25 View
510(k) K213319 Viz ANEURYSM, Viz ANXQFM2022-02-18 View
510(k) K210209 Viz ICHQAS2021-03-23 View
510(k) K193658 Viz ICHQAS2020-03-18 View
510(k) K180161 Viz CTPLLZ2018-04-20 View