43 results · 24ms · Sources: EU EUDAMED, US FDA

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ROSA ONE Brain application

FDA 510(k)
FDA Class 2 ·Neurology

ReLine

FDA UDI
Nuvasive, Inc.·00195377047502·RELINE-O Trial, 7mm H Offset Right L-pop

Zavation

FDA UDI
Zavation LLC·00842166131675·Ti3Z CIF 12mmx14mmx11mm -5 deg

Screwdriver

FDA UDI
Treace Medical Concepts, Inc.·00810111226615·Cannulated Screwdriver

OsteoMed

FDA UDI
OSTEOMED LLC·00845694006729·Drill Guide, Compression, Blunt Cannula

ELMED

FDA UDI
ELMED INCORPORATED·00842180107762·FOOTSWITCH, SINGLE, WATER-SEALED, FOR ELMED ESU...

Orfit

FDA UDI
Orfit Industries NV·05420028754139·

NA

FDA UDI
Biedermann Motech GmbH & Co. KG·04250869692755·MOSS VRS Spannschlüssel Approximator HP

MICROSCAN SYNERGIES PLUS

FDA 510(k)
FDA Class 2 ·Microbiology

MODIFICATION TO ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, ARTHROWANDS AND SPINE WANDS

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

AMT RIGHT ANGLE EXTENSION 12"

FDA Adverse Event
Injury ·APPLIED MEDICAL TECHNOLOGY, INC·Product code KNT·December 28, 2020

LIGHTSHEER (ALL MODELS)

FDA Adverse Event
Injury ·*·Product code GEX·March 2, 2006

SPRINT FIDELIS

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code LWS·February 8, 2014

CONSULTA CRT-D

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·April 10, 2013

DEEP BRAIN STIMULATION DEVICE

FDA Adverse Event
Other ·MEDTRONIC NEUROMODULATION·Product code MHY·September 21, 2007

COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

STOCKERT 70 RF GENERATOR

FDA Adverse Event
Injury ·STOCKERT GMBH·Product code DRF·August 11, 2011

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
Malfunction ·INVAMEX·Product code IOR·July 1, 2013

V.A.C. THERAPY

FDA Adverse Event
Injury ·KCI USA INC.·Product code OMP·February 23, 2015

V.A.C. THERAPY

FDA Adverse Event
Injury ·KCI USA INC.·Product code OMP·February 23, 2015