16 results · 22ms · Sources: EU EUDAMED, US FDA

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BRIGHTWAY BRAND NITRILE SURGICAL GLOVES - STERILE (POWDERED)

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

Arthrex®

FDA UDI
ARTHREX, INC.·00888867400917·1.9mm Snap-off FT Pin 40mm

11G BLADED MAMMOTOME ST PROBE

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.·Product code KNW·February 27, 2006

Palm NRG cellulite and muscle toning body device

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

MAGPRO, MODELS R30 WITH MAGOPTION, X100, X100 WITH MAGOPTION

FDA 510(k)
FDA Class 2 ·Neurology

MAMMOTOME CONTROL MODULES

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006

MAMMOTOME CONTROL MODULES

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 13, 2006

MAMMOTOME HARDWARE HOLSTER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006

MAMMOTOME CONTROL MODULES

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 13, 2006

MAMMOTOME CONTROL MODULES

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006

MENTOR MEMORYGEL BREAST IMPLANT

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FTR·December 5, 2024

MAMMOTOME CONTROL MODULES

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 14, 2006

MAMMOTOME CONTROL MODULES

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code KNW·June 13, 2006

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 7, 2013

CONSERVE(R) TOTAL A-CLASS

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDL·February 15, 2011

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014