Seigla Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seigla Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LiquID .051 LP Guide Catheter Extension, LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension
2
Total
2
Cleared
0
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) Regulatory Record - Seigla Medical, Inc.
2 devices