849 results · 29ms · Sources: EU EUDAMED, US FDA

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ACUBAND ACUPRESSURE WRIST BAND DEVICE

FDA 510(k)
FDA Unclassified ·Unknown

JOBST forMen

FDA UDI
BSN MEDICAL, INC.·04042809843767·FOR MEN 30-40 MM HG KNEE HIGH CLOSED TOE EXTRA ...

ARx SAI

FDA UDI
Life Spine, Inc.·00190837196004·

Arx

FDA UDI
Life Spine, Inc.·00190837175528·

DBB-05 HEMODIALYSIS DELIVERY SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

FLEXICAST

FDA 510(k)
FDA Class 2 ·Dental

1.3MM TI CRTX SCREW SLF-DRLG W/PLUSDRIVE(TM) RECESS 6MM

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code DZL·April 11, 2013

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LDD·May 28, 2008

VIRTUOSO DR

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·April 13, 2011

UNKNOWN

FDA Adverse Event
Malfunction ·COOK, INC.·Product code DTK·August 21, 2014

UNK

FDA Adverse Event
Injury ·COOK, INC.·Product code DTK·August 20, 2014

UNKNOWN

FDA Adverse Event
Injury ·COOK INC·Product code DTK·August 20, 2014

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 26, 2012

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 13, 2010

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 7, 2010

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 16, 2011

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 23, 2011

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 28, 2011

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 27, 2012

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 17, 2012