Medical Device Manufacturer · US , Buffalo , MN

Seigla Medical, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022

Total

Cleared

Denied

Seigla Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Buffalo, US.

Latest FDA clearance: Apr 2025. Active since 2022. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Seigla Medical, Inc.

2 devices

1-2 of 2