21 results · 31ms · Sources: EU EUDAMED, US FDA

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ROYALE BRAND LATEX CONDOMS (SILICONE)-COLORED/ASSORTED COLORS

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

NA

FDA UDI
KEY SURGICAL, INC.·10849771049040·K-Wires, Single trocar, .045-inch (1.1mm) diame...

Key Surgical K-Wires and Steinmann Pins

FDA UDI
KEY SURGICAL, INC.·00849771012467·K-Wires, Single trocar, .045-inch (1.1mm) diame...

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·14026704912374·

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704292695·

K-Wire w. trocar/round end 1.14mm/102mm, 6 pcs./unit

FDA UDI
mahe medical gmbh·EMAHKM711320·K-Wire w. trocar/round end 1.14mm...

mahe medical GmbH

FDA UDI
mahe medical gmbh·04050659484238·K-Wire w. trocar/round end _x000D_...

G8 AUTOMATED HPLC ANALYZER, MODEL HLC-723 G8

FDA 510(k)
FDA Class 2 ·Hematology

Carefusion NeutraClear Needle-free connector

FDA 510(k)
FDA Class 2 ·General Hospital

INRATIO PT/INR TEST STRIP

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·April 29, 2014

PLUM 1.6 W/ DATAPORT

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 1, 2013

NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·COCHLEAR LTD.·Product code MCM·January 26, 2011

LINER NEUTRAL 36 MM I.D. SIZE NN FOR USE WITH 62 MM O.D. SIZE NN SHELL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 25, 2019

TOSOH HLC-723G8 ANALYZER

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

TOSOH HLC-723G8 ANALYZER

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·December 15, 2017

TOSOH HLC-723G8 ANALYZER

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

TOSOH HLC-723G8 ANALYZER

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·December 11, 2017

TOSOH HLC-723G8 ANALYZER G8

FDA Adverse Event
Injury ·TOSOH CORPORATION·Product code LCP·January 5, 2016

TOSOH HLC-723G8 ANALYZER G8

FDA Adverse Event
Injury ·TOSOH CORPORATION·Product code LCP·January 3, 2017

IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·November 28, 2023