26 results · 33ms · Sources: EU EUDAMED, US FDA

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INFARED EAR THERMOMETER, MODEL TH8 SERIES

FDA 510(k)
FDA Class 2 ·General Hospital

Beaver Visitec Inter

FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918185361·Eye Fluid Wick_0.4x15cm_Non-sterile_3000EA/CS

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033220672·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033220726·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033221891·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033220719·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033220665·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033220689·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033220658·

InTess C Cervical Cage System

FDA UDI
Kalitec Direct LLC·B07309K01105N0·Cervical Trial, 14 x 11, 5mm, 0 Degree, No Taper

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033220702·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033220696·

ENGPLUS

FDA 510(k)
FDA Class 2 ·Neurology

NORMOCARB STERILE BICARBONATE RENAL DIALYSIS

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

SYRINGE 20ML LL CONVENIENCE TRAY EUROPE

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 15, 2021

UNIVERSAL SCREWDRIVER HANDLE

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·December 2, 2024

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·January 27, 2012

TSRH SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code MNI·April 16, 2013

BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

FDA Adverse Event
Malfunction ·BD (SUZHOU)·Product code FOZ·July 20, 2022

SPEEDBAND SUPERVIEW SUPER 7¿

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code MND·March 19, 2013