28 results · 33ms · Sources: EU EUDAMED, US FDA

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POWERHEART AED G3 (MODEL 9390E), POWERHEART AED G3 AUTOMATIC (MODEL 9390A)

FDA 510(k)
FDA Class 3 ·Cardiovascular

HairCheck-DT (Amphetamines)

FDA UDI
Quest Diagnostics·00868586000230·HairCheck-DT (Amphetamines) is an ELISA test ki...

Slide Attachment SG

FDA UDI
Cendres+Métaux SA·07640173092049·Slide Attachment SG Activating screw O

JOBST forMen

FDA UDI
BSN MEDICAL, INC.·04042809849820·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE MEDIUM K...

FLEX-NAILS

FDA 510(k)
FDA Class 2 ·Orthopedic

MODIFICATION TO COULTER LH 750 HEMATOLOGY ANALYZER, MODEL 6605632

FDA 510(k)
FDA Class 2 ·Hematology

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120291·16mm x 13.5mm x 11mm 2° Lordotic Trial/Broach w...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120284·16mm x 13.5mm x 10mm 2° Lordotic Trial/Broach w...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120307·16mm x 13.5mm x 12mm 2° Lordotic Trial/Broach w...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120246·16mm x 13.5mm x 6mm 2° Lordotic Trial/Broach w/...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120277·16mm x 13.5mm x 9mm 2° Lordotic Trial/Broach w/...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120253·16mm x 13.5mm x 7mm 2° Lordotic Trial/Broach w/...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120260·16mm x 13.5mm x 8mm 2° Lordotic Trial/Broach w/...

MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code LXH·March 31, 2010

XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Death ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·November 19, 2009

SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·July 3, 2018

GORE® PROPATEN® VASCULAR GRAFT

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·March 16, 2021

MICRO CHPV W RICKHAM UNITIZED

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·April 11, 2013

EASYTRAK 3

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code OJX·April 12, 2011

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORP.·Product code LZG·March 24, 2008