31 results · 23ms · Sources: EU EUDAMED, US FDA

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ACTABOND Topical Skin Adhesive

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

HUDSON 22MM DUAL HTD CIRC KIT

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BTT·February 19, 2016

HUDSON 22MM DUAL HTD CIRC KIT

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BTT·February 19, 2016

HUDSON 22MM DUAL HTD CIRC KIT

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BTT·February 19, 2016

HUDSON 22MM DUAL HTD CIRC KIT

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BTT·February 19, 2016

CoRoent

FDA UDI
Nuvasive, Inc.·00887517291998·CoRoent® XLFW, 10x22x50mm

LoFric® Sense™

FDA UDI
Wellspect AB·07333387021881·Single Use Urinary Catheter LoFric Sense Nelato...

LoFric® Sense™

FDA UDI
Wellspect AB·07392532086168·Single Use Urinary Catheter LoFric Sense Nelato...

CoRoent

FDA UDI
Nuvasive, Inc.·00887517731029·CoRoent XL+, 10x18x50mm 15°

MEGA SPINE SYSTEM

FDA UDI
BK MEDITECH CO.,LTD.·08809763501296·Mono Screw Driver

A.D. Protraction

FDA UDI
ORMCO CORPORATION·00889989060003·International Face Mask Blue

Vilex Power Accessory

FDA UDI
VILEX IN TENNESSEE, INC.·00841731122254·KWire .062x4" (1.6x100mm)

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523104024·T³ Acetabular Hemispherical Shell, Cluster Hole...

GYNECARE MORCELLEX TISSUE MORCELLATOR, MODELS MX0100 AND MX0100R

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

ESOPHAGEAL / RECTAL TEMPERATURE PROBE, 9FR, 12FR, ESOPHAGEAL STETHOSCOPE WITH TEMPERATURE SENSOR, 9FR, 12FR, 18FR, 24FR

FDA 510(k)
FDA Class 2 ·Anesthesiology

CARELINK

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code MMI·June 17, 2011

COMP RVRS SHLDR GLNSP +6 36MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·December 12, 2018

ARCOM XL 44-36 RTNV+3 HMRL BRG

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·December 12, 2018