Medical Device Manufacturer · US , Sunnyvale , CA

Redwood Biotech, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1999

Total

Cleared

Denied

Redwood Biotech, Inc. has 6 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 6 cleared submissions from 1999 to 2000. Primary specialty: Toxicology.

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

Redwood Biotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Redwood Biotech, Inc.

6 devices

1-6 of 6