Medical Device Manufacturer · US , Mountain View , CA

Updoc, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025

Total

Cleared

Denied

FDA 510(k) Regulatory Record - Updoc, Inc. Chemistry ✕

1 devices

1-1 of 1

PCCP authorized FDA software change control pathway

Regulatory consultant 510(k) submission support ecosystem

RQM+

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026