12 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SCINITREX BLUE POWDERED NITRILE EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ARCHITECT 2nd Generation Testosterone
FDA 510(k)
FDA Class 1
·Clinical Chemistry
BARD LARGE PORE SOFT MESH AND SOFT MESH PRESHAPED
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
COLLECT.NO.QAS KNEE IMPLANTS ROTAT.HINGE
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·May 12, 2021
CAPSUREFIX
FDA Adverse Event
Injury
·MPRI·Product code DTB·February 9, 2013
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·January 7, 2011
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 12, 2014
COLLECT.NO.QAS KNEE IMPLANTS ROTAT.HINGE
FDA Adverse Event
Injury
·AESCULAP AG·Product code KRO·December 1, 2021
AS ENDURO FEMORAL COMPONENT CEMENTED F1R
FDA Adverse Event
Injury
·AESCULAP AG·Product code JWH·September 1, 2021
ENDURO MENISCAL COMPONENT F3 10MM
FDA Adverse Event
Injury
·AESCULAP AG·Product code KRO·August 4, 2021
COLLECT.NO.QAS KNEE IMPLANTS ROTAT.HINGE
FDA Adverse Event
Injury
·AESCULAP AG·Product code HRZ·August 10, 2022
ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020