16 results · 20ms · Sources: EU EUDAMED, US FDA

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PROFEMUR Z REVISION HIP STEM

FDA 510(k)
FDA Class 3 ·Orthopedic

ArgenZ HT+ 95x22 B3

FDA UDI
ARGEN CORPORATION, THE·D818122778·Dental porcelain/ceramic restoration kit

CELLAVISION DM1200 WITH THE BODY FLUID APPLICTION

FDA 510(k)
FDA Class 2 ·Hematology

MODIFICATION TO TSRH SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

SCREW, UNKNOWN TYPE

FDA Adverse Event
Malfunction ·ZIMMER BIOMET SPINE INC.·Product code KWP·June 17, 2019

SCREW, UNKNOWN TYPE

FDA Adverse Event
Malfunction ·ZIMMER BIOMET SPINE INC.·Product code KWP·June 17, 2019

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012

TSRH® SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 5, 2016

TSRH® SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 5, 2016

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

ADVIA CENTAUR CP

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·September 26, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 14, 2011

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 13, 2012

UNKNOWN_NEUROVASCULAR_PRODUCT

FDA Adverse Event
Death ·CONCENTRIC MEDICAL·Product code NRY·December 18, 2012