324 results · 23ms · Sources: EU EUDAMED, 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