40 results · 29ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

TQ HBA1C GEN3

FDA 510(k)
FDA Class 2 ·Hematology

N/A

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169373341·BLADE 5102914 29MM WIDE VESSELBLADE 14CM

CRYOPEN CRYOSURGICAL SYSTEM, K102214

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

LEONE SPA

FDA UDI
LEONE SPA·08033707094937·IMPLANT 2.9 W/CAPS D2,9 L14MM

LEONE SPA

FDA UDI
LEONE SPA·08033707094555·IMPLANT 2.9 W/CAP D2,9 L14MM

Monster® Screw System

FDA UDI
Paragon 28, Inc.·00889795040633·Drill, 2.9 x 140mm, Cannulated, 3/16" Sq. Conne...

Paragon 28

FDA UDI
Provision·B504OMP9911029140·

Plateau Spacer System

FDA UDI
Life Spine, Inc.·00190837026912·PLATEAU Interbody, Curved, Bulleted, 11mm 29mm ...

TENS STIMULATOR, MODELS 2800 AND 3000

FDA 510(k)
FDA Class 2 ·Neurology

SONICWAVE SONIC PLAQUE REMOVER

FDA 510(k)
FDA Class 1 ·Dental

HLM TUBING SET

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 1, 2015

VKMO 70000 #QUADROX-I HMO 70000+VHK71

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 23, 2015

BO-HQV 70600#ADULT PACK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 19, 2015

BO-HQV #70600ADULT PACK

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY AG·Product code DTN·March 4, 2015

BO-HQV 70600#ADULT PACK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·March 27, 2015

BO-HQV 70600#ADULT PACK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·April 9, 2015

VKMO 11000

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 24, 2015

BO-HQV 70600 ADULT PACK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·July 15, 2015

RESERVOIR VHK

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·July 28, 2015

VENOUS HARDSHELL CARDIOTOMY RESERVOIR

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTM·September 13, 2016