VPIX Medical, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
VPIX Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: cCeLL - In vivo with Drop-In Robo (CN100-2W2C488775, CN100-1W1C775, DR200), cCeLL - In vivo
2
Total
2
Cleared
0
Denied
VPIX Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Daejeon, KR.
Latest FDA clearance: Feb 2026. Active since 2024. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by VPIX Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRC Global, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - VPIX Medical, Inc.
2 devices