Updoc, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Updoc, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UpDoc
1
Total
1
Cleared
0
Denied
Updoc, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Updoc, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant. 1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Updoc, Inc.
1 devices