16 results · 27ms · Sources: EU EUDAMED, US FDA

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POLYVIOLENE(TM) SUTURE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

EZPass™

FDA UDI
Biomet Orthopedics, LLC·00887868511035·

EZ PASS

FDA UDI
Biomet Orthopedics, LLC·00880304563759·

EZ PASS 70 DEGREE LEFT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWQ·February 2, 2018

EZ PASS 70 DEGREE LEFT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWQ·February 2, 2018

KESTREL LENS CASE 1543-893S/P-1700-2611

FDA 510(k)
FDA Class 2 ·Ophthalmic

MODIFCATION TO: NUVASIVE NEUROVISION EMG ENDOTRACHEAL TUBE

FDA 510(k)
FDA Class 2 ·Neurology

EZ PASS 70 DEGREE LEFT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWQ·February 2, 2018

EZ PASS 70 DEGREE LEFT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWQ·December 19, 2017

EZ PASS 70 DEGREE LEFT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWQ·December 19, 2017

EZPass Passer, Sterile single use arthroscopic instrument utilized in conjunction with a nitinol wire to aid in passing suture through soft tissue. Part numbers 904050, 904051, 904052, 904053, 904054, 904055, and 904056.

FDA Enforcement
Class II ·Terminated·Biomet, Inc.·June 25, 2014

MULTI-LUMEN PI CVC KIT: 3-L 7 FR X 8IN (2

FDA Adverse Event
Malfunction ·ARROW INTL., INC.·Product code FOZ·January 3, 2013

TOTALCARE SPO2RT

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·November 12, 2010

OT PING ENHANCED METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 1, 2014

EZ PASS 30 DEGREE LEFT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code HWQ·May 7, 2018

EZPass Passer, Sterile single use arthroscopic instrument utilized in conjunction with a nitinol wire to aid in passing suture through soft tissue. Part numbers 904050, 904051, 904052, 904053, 904054, 904055, and 904056.

FDA Recall
Terminated ·Biomet, Inc.·Product code HWQ·April 15, 2014