41 results · 39ms · Sources: EU EUDAMED, US FDA

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UTERINE INJECTOR

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496022503·NAOMI 30, SIZE XXL, NERO, GRADUATED COMPRESSION...

METAL SCREW ANCHOR

FDA 510(k)
FDA Class 2 ·Orthopedic

FETALGARD LITE

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

RESOLUTION 360 CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·December 2, 2024

RESOLUTION 360 CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·October 9, 2025

RESOLUTION CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·June 17, 2025

RESOLUTION 360 CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·November 25, 2024

RESOLUTION CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·January 8, 2025

RESOLUTION 360 CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·March 6, 2025

RESOLUTION CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·June 11, 2025

RESOLUTION CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·February 13, 2025

RESOLUTION 360 CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·January 8, 2025

RESOLUTION 360 CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·March 4, 2025

RESOLUTION CLIP

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code PKL·March 28, 2025

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON INC·Product code OTN·March 27, 2013

PIC 50

FDA Adverse Event
Malfunction ·WELCH ALLYN PROTOCOL, INC·Product code MKJ·February 15, 2011

PALL TRANSFER/FREEZING BAG SET

FDA Adverse Event
Malfunction ·ENTASEC S.A. DE C.V.·Product code KSR·April 3, 2008

IMMULITE 2000

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code CFP·January 23, 2012

FREESTYLE FREEDOM LITE

FDA Adverse Event
Injury ·Product code NBW·February 15, 2011