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

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FLAVORED MALE LATEX CONDOM

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

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·00304040015322·Zirlux 16+ D3 85x40x22

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·00304040005156·Maxitest Biological Monitor

PULSE GEN MODEL UNK

FDA Adverse Event
Injury ·CYBERONICS·Product code LYJ·February 16, 2012

Cosmolock

FDA UDI
Kalitec Direct LLC·B07311K0112230·Tap, 5.50mm, Cannulated, Fixed Sleeve

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254448·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254530·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254479·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254431·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254516·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254462·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254509·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254486·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254523·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254493·

SOFIA VERGARA

FDA UDI
FGX INTERNATIONAL INC.·00193033254455·

ANGIO FLOW THERMODILUTION CATHETER, MODEL AF-CATH-01; ANGIOFLOW METER, MODELS HQ100 AND HQ101

FDA 510(k)
FDA Class 2 ·Cardiovascular

SURGITRON IEC II

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

SYNCHRON LX 20 PRO CLINICAL SYSTEMS

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·June 8, 2011

ACCU-CHEK ® AVIVA PLUS TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 19, 2013