17 results · 31ms · Sources: EU EUDAMED, US FDA

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Diode laser hair removal device

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MAESTRO TOTAL WRIST

FDA UDI
Biomet Orthopedics, LLC·00880304479579·

Maestro™ Total Wrist

FDA UDI
Biomet Orthopedics, LLC·00887868239786·

LTM-T SURGICAL MESH

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SPINEWAND SURGICAL DEVICE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SOF-FLEX MULTI-LENGTH URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·October 24, 2024

RUSCH TRULED RECHARGEABLE HANDLE SET

FDA Adverse Event
Malfunction ·TELEFLEX·Product code GCI·October 15, 2014

GYNECARE PROLIFT TOTAL PELVIC FLOOR REPAIR SYSTEM

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTP·June 20, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Injury ·ANIMAS CORPORATION·Product code LZG·July 27, 2011

SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·September 30, 2024

SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·October 7, 2024

SOF-FLEX MULTI-LENGTH URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·October 21, 2024

SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·April 19, 2021

SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Injury ·COOK INC·Product code FAD·April 19, 2021

SOF-FLEX PEDIATRIC DOUBLE PIGTAIL URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·June 28, 2022

VITEK® 2 AST-P656 TEST KIT

FDA Adverse Event
Malfunction ·BIOMERIEUX, INC.·Product code LON·December 18, 2018

SOF-FLEX MULTI-LENGTH URETERAL STENT SET

FDA Adverse Event
Malfunction ·COOK INC·Product code FAD·October 21, 2024