324 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UNICRYL QUICK
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
REPROCESSED TROCARS AND CANNULAS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
RADIAL HEAD IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·ZIMVIE US CORP LLC·Product code DZE·March 12, 2026
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026
ACCU-CHEK ® ULTRAFLEX INFUSION SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·April 23, 2013
NI
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·April 22, 2011
ATTAIN OTW
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWP·July 10, 2008
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·March 23, 2018
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·March 23, 2018
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·March 23, 2018
CERTAIN GOLD-TITE LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026
CERTAIN GOLD-TITE LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·February 13, 2020
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·March 23, 2018
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·March 23, 2018
WAVEWRITER ALPHA? PRIME 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 20, 2026