16 results · 21ms · Sources: EU EUDAMED, US FDA

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SERFAS, SERFAS GENERATOR, SERFAS CONSOLE, SERFAS PROBE, SERFAS HANDPIECE CABLE, SERFAS FOOTSWITCH

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

11G BLADED MAMMOTOME ST PROBE

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

VYSIS EGR1 FISH PROBE KIT (VYSIS LSI EGR1 SPECTRUM/ORANGE/D5S23, D5S721, SPECTRUM GREEN PROBE), MODEL 4N37-020

FDA 510(k)
FDA Class 2 ·Immunology

Arthrex Univers Revers Modular Glenoid System

FDA 510(k)
FDA Class 2 ·Orthopedic

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

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 VERIO IQ METER

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

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·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

COMPRESS 4 BOLT CONCENTRC CLMP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HSD·December 3, 2018

COMP RVRS SHLDR GLNSP STD 41MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PAO·May 16, 2018