268 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SEQUOIA SPINAL SYSTEM, MODEL 3300 SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
VYPRO MESH, VICRYL PROLENE PARTIALLY ABSORBABLE SYNTHETIC SURGICAL MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BOSS-2000-2 VACUUM ERECTION DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
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
BONE REDUCTION FORCEPS-LARGE
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HTD·April 23, 2013
CHOICE GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - COSTA RICA·Product code DQX·April 29, 2011
CAPSURE SP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·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
CERTAIN® TITANIUM LARGE HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code DZE·February 25, 2022