Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) 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 — 11 products

Total Devices11
Categories5
Latest Approval2025-06-10
TypeNumberDevice NameCodeDate
510(k) K250354 Viz Subdural+, Viz SUBDURAL PLUS QIH 2025-06-10 View
510(k) K232363 Viz HDS, Viz Volume Plus, Viz ICH+ QIH 2024-02-05 View
510(k) DEN230003 Viz HCM QXO 2023-08-03 View
510(k) K223443 Viz AAA QFM 2023-03-17 View
510(k) K223042 Viz LVO ContaCT QAS 2022-10-21 View
510(k) K221100 Viz RV/LV QIH 2022-08-29 View
510(k) K220439 Viz SDH QAS 2022-07-25 View
510(k) K213319 Viz ANEURYSM, Viz ANX QFM 2022-02-18 View
510(k) K210209 Viz ICH QAS 2021-03-23 View
510(k) K193658 Viz ICH QAS 2020-03-18 View
510(k) K180161 Viz CTP LLZ 2018-04-20 View
↑