1,953 results · 31ms · Sources: EU EUDAMED, US FDA

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GE DATEX-OHMEDA AISYS

FDA 510(k)
FDA Class 2 ·Anesthesiology

Humelock II Cementless Shoulder System

FDA UDI
FX SOLUTIONS·03701037301074·HUMELOCK II STEM TA6V SIZE 13 CEMENTLESS TI/HA

OsteoMed

FDA UDI
OSTEOMED LLC·00845694040235·PrimaLIF 13mm Paddle Shaver

Straight Plate, 3.5mm

FDA UDI
I.T.S. GmbH·09120034304699·Straight Plate, 3.5mm, 13-Hole

LUMANOSITY CELEBRITY, MODEL 204

FDA 510(k)
FDA Class 2 ·Physical Medicine

MODIFICATION TO CAVERMAP SURGICAL AID

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

RETROFLEX 3/SAPIEN DELIVERY SYSTEM

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code NPT·May 13, 2013

PERSONA TIBIAL ARTICULAR SURFACE INSERTER

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code JWH·September 11, 2014

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 20, 2011

YAMATO PLUS-R 7.5FR. 30CC IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 4, 2021

YAMATO PLUS-R 7.5FR. 35CC IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·July 8, 2021

TRANS-RAY PLUS 7.5 FR. 40CC IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·August 26, 2021

TRANS-RAY PLUS 7.5 FR. 40CC IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·September 1, 2021

BLOWER MISTER, 5-PACK

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code FQH·May 28, 2021

TRANS-RAY 7FR. 40CC IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·July 16, 2021

TRANS-RAY PLUS 7.5 FR. 40CC IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·September 21, 2021

HSK III SYSTEM (3.8MM)

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code DXC·August 12, 2021

TRANS-RAY 7FR. 40CC IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·July 8, 2021

HEMOPRO2 EXTENSION CABLE

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code GEI·June 18, 2021

HST III SYSTEM (4.3MM)

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR LLC·Product code DXC·November 16, 2021