297 results
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41ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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C7 ANTERIOR CERVICAL INTERVERTEBRAL FUSION CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
CoRoent
FDA UDI
Nuvasive, Inc.·00887517577245·CoRoent Ant TLIF PEEK, 12x11x32mm 0°
DD tempMED
FDA UDI
Dental Direkt GmbH·EDDIK113201·DD tempMED are pre-colored dental milling blank...
Z Liquid HT B2-S 100ml
FDA UDI
ARGEN CORPORATION, THE·D818121320·Dental porcelain/ceramic restoration kit
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321213200·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311213200·
MEYERHOEFER-CHALAZION CURETTE
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896012981·MEYERHOEFER-CHALAZION CURETTE
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515016590·Mayo Hegar NH, stubby jaw, 6 1/4"
VASOVAPOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
GLOBALCARDIO
FDA 510(k)
FDA Class 2
·Cardiovascular
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197040747·Super-Cut Endarterectomy Scissors
full c...
ACCENT DR.
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC CRMD·Product code DXY·January 13, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
ASR ACETABULAR IMPLANT 60
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·June 1, 2011
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026