7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RUBBER BAND, STERILE
FDA 510(k)
FDA Class 1
·Dental
Pigtail Ureteral Catheter Set, Sof-Flex AQ Coated Pigtail Ureteral Catheter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DATASON RTL II
FDA 510(k)
FDA Class 2
·Radiology
ENDEAVOR SPRINT OTW
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·June 19, 2014
MESHGRAFT II DERMATOME WITH RATCHET
FDA Adverse Event
Malfunction
·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code GFD·October 13, 2010
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·December 20, 2012
CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026