Medical Device Manufacturer · US , Sunnyvale , CA

R2 Technology, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2002

Total

Cleared

Denied

R2 Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 5 cleared submissions from 2002 to 2005. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by R2 Technology, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.

R2 Technology, Inc. is one of 23674 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - R2 Technology, Inc.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 25, 2026