36 results · 23ms · Sources: EU EUDAMED, US FDA

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GLOBAL HEALTHCARE VAGINAL SPECULUM

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

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033519899·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033519905·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033519936·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033519912·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033519950·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033519929·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033519943·

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012979·PedFuse Remind LES, Quad-H, 7.0mm x 35mm

POSI-GRIP UMBILICAL CORD CLAMP, STERILE, MODEL 384, POSI-GRIP UMBILICAL CORD CLAMP, NON-STERILE, MODEL 385

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

JAS MAGNESIUM REAGENT

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

HEALONID GV

FDA Adverse Event
Injury ·PHARMACIA & UPJOHN, FYRISLUND·Product code LZP·December 27, 2001

CAPSUREFIX NOVUS

FDA Adverse Event
Death ·MPRI·Product code DTB·March 20, 2013

VIBRANT SOUNDBRIDGE

FDA Adverse Event
Malfunction ·VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Product code MPV·February 4, 2011

SUMMIT 2.0MM HEX DRIVER SHAFT

FDA Adverse Event
Malfunction ·DEPUY SPINE, INC.·Product code LXH·March 14, 2008

METASUL, ALPHA INSERT, II/32

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·March 15, 2018

METASUL, ALPHA INSERT, II/32

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·June 25, 2018

DURASUL, ALPHA INSERT, KK/36

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LZO·March 6, 2018

DURASUL, ALPHA INSERT, HOODED, MM/28

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code JDI·May 22, 2018

DURASUL, ALPHA INSERT, HH/32

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LZO·June 4, 2018