17 results · 35ms · Sources: EU EUDAMED, US FDA

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ELECTROENCEPHALOGRAPHS EEG-5208,5210

FDA 510(k)
FDA Class 2 ·Neurology

Ultraverse® 018

FDA UDI
Bard Peripheral Vascular, Inc.·00801741156557·Ultraverse® 018 PTA Balloon Dilatation Catheter...

NAR

FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209128549·

POWDER FREE NITRILE PATIENT EXAMINATION GLOVE, BLUE, WHITE AND GREEN COLORED. NON-STERILE, LOW DERMATITIS POTENTIAL

FDA 510(k)
FDA Class 1 ·General Hospital

Medical Nitrile Examination Gloves

FDA 510(k)
FDA Class 1 ·General Hospital

NA

FDA UDI
STRYKER CORPORATION·04546540362377·1.6mm Cross-Cut Fissure Extended

NA

FDA UDI
STRYKER CORPORATION·04546540362346·1.2mm Cross-Cut Fissure

NA

FDA UDI
STRYKER CORPORATION·04546540362360·2.1mm Cross-Cut Fissure

NA

FDA UDI
STRYKER CORPORATION·04546540467638·3.2mm Cross-Cut Fissure Extended

NA

FDA UDI
STRYKER CORPORATION·04546540362353·1.6mm Cross-Cut Fissure

NA

FDA UDI
STRYKER CORPORATION·04546540362384·2.1mm Cross-Cut Fissure Extended

NA

FDA UDI
STRYKER CORPORATION·04546540362339·1.0mm Cross-Cut Fissure

*

FDA Adverse Event
Malfunction ·COVIDIEN·Product code LWH·April 24, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 5, 2012

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 23, 2010

1.2mm Cross Cut Fissure - Intended for use in the cutting, drilling, reaming, decorticating, shaping and smoothing of bone, bone cement and teeth in a variety of surgical procedures including but not limited to dental, ENT (ear, nose and throat), neuro, spine and endoscopic applications Catalog Number: 5820-066-012

FDA Enforcement
Class II ·Ongoing·Stryker Corporation·October 23, 2024

1.2mm Cross Cut Fissure - Intended for use in the cutting, drilling, reaming, decorticating, shaping and smoothing of bone, bone cement and teeth in a variety of surgical procedures including but not limited to dental, ENT (ear, nose and throat), neuro, spine and endoscopic applications Catalog Number: 5820-066-012

FDA Recall
Open, Classified ·Stryker Corporation·Product code HBE·September 5, 2024