Atlas FDA

IDEV Technologies, Inc.

2 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch IDEV Technologies, Inc.

RecordFirmDate
IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Bili recall (Z-1550-2013)IDEV Technologies, Inc.2013-06-18
SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Intend recall (Z-1213-2012)Idev Technologies, Inc.2012-03-15

Track IDEV Technologies, Inc. automatically

Every clearance here is in the API, with alerts when new ones post.