Medical Device Manufacturer · US , Bethesda , MD

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

3 submissions · 3 cleared · Since 1996

Total

Cleared

Denied

Sienna Biotech, Inc. has 3 FDA 510(k) cleared medical devices. Based in Bethesda, US.

Historical record: 3 cleared submissions from 1996 to 1997. Primary specialty: Microbiology.

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

Sienna 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 - Sienna Biotech, Inc.

3 devices

1-3 of 3

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 28, 2026