8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
SURGICAL SCALPEL BLADES & DISPOSABLES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MODEL 503FB
FDA 510(k)OPHTHALMIC TABLE
FDA 510(k)
FDA Class 1
·Ophthalmic
VIPER MIS SINGLE INNER SETSCW
FDA Adverse Event
Injury
·DEPUY SYNTHES SPINE·Product code NKB·June 3, 2014
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 26, 2012
NATURAL KNEE II STEMMED TIBIAL BASEPLATE
FDA Adverse Event
Malfunction
·ZIMMER, INC.·Product code JWH·September 23, 2010
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021
Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018