Medical Device Manufacturer · DE , 91074 Herzogenaurach

Seiratherm GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Seiratherm GmbH has 1 FDA 510(k) cleared medical devices. Based in 91074 Herzogenaurach, DE.

Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Seiratherm GmbH Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Seiratherm GmbH

1 devices

1-1 of 1

Data Source

Sourced from the FDA 510(k) public files . 174,477 total devices indexed.

Last updated: Mar 22, 2026