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

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ComfortGuard Surgical Gown, i600, Film Reinforced

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

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575172344·Knee femur prosthesis trial - Megasystem-C Tumo...

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575172313·Knee femur prosthesis trial - Megasystem-C Tumo...

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575180264·Knee femur prosthesis trial - Megasystem-C Tumo...

LINK Instruments - Trial implants and size gauges

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575180271·Knee femur prosthesis trial - Megasystem-C Tumo...

GM HELIX ACQUA IMPLANT,TI,5.0X16

FDA Adverse Event
Injury ·NEODENT - JJGC S.A.·Product code DZE·May 16, 2018

HEIDELBERG RETINA ANGIOGRAPH 2/OPTICAL COHERENCE TOMOGRAPH, MODEL HRA 2/OCT

FDA 510(k)
FDA Class 2 ·Ophthalmic

QUADROX-I PEDIATRIC MICROPOROUS MEMBRANE OXYGENATOR WITH INTEGRATED ARTERIAL FILTER WITH SOFTLINE / BIOLINE COATING

FDA 510(k)
FDA Class 2 ·Cardiovascular

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA Adverse Event
Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·March 22, 2020

GM HELIX IMPLANT 4.3X13

FDA Adverse Event
Injury ·NEODENT - JJGC S.A.·Product code DZE·June 6, 2018

GM HELIX IMPLANT 4.3X13

FDA Adverse Event
Injury ·NEODENT - JJGC S.A.·Product code DZE·June 22, 2018

GM DRIVE ACQUA IMPLANT 3.5X8 MM

FDA Adverse Event
Injury ·NEODENT - JJGC S.A.·Product code DZE·August 29, 2018

GM HELIX ACQUA IMPLANT 3.75X11.5

FDA Adverse Event
Injury ·NEODENT - JJGC S.A.·Product code DZE·April 24, 2018

GM HELIX IMPLANT 3.5X10

FDA Adverse Event
Injury ·NEODENT - JJGC S.A.·Product code DZE·June 29, 2018

GM HELIX ACQUA IMPLANT 3.5X11.5

FDA Adverse Event
Injury ·NEODENT - JJGC S.A.·Product code DZE·April 24, 2018

GM DRIVE IMPLANT 3.5X10

FDA Adverse Event
Injury ·NEODENT - JJGC S.A.·Product code DZE·April 20, 2018

CAPSURE

FDA Adverse Event
Injury ·MPRI·Product code DTB·October 10, 2014

CAPSUREFIX NOVUS

FDA Adverse Event
Death ·MPRI·Product code DTB·June 11, 2013

UNKNOWN DEPUY ASR FEMORAL HEAD

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KXA·July 8, 2011

COOK® SINGLE-USE HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·COOK INC·Product code GEX·May 17, 2019