27 results · 22ms · Sources: EU EUDAMED, US FDA

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QUANTA LITE GPA (GASTRIC PARIETAL CELL ANTIBODY) ELISA

FDA 510(k)
FDA Class 2 ·Immunology

Zirlux

FDA UDI
HENRY SCHEIN, INC.·H65890105580·Zirlux Titanium Screw compatible with: Nobel Bi...

Endo Carry-on Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964150999·Endo Carry-on Procedure Kit contains Basin, VIA...

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033169063·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033169094·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033169070·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033169100·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033169087·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033169117·

SYNOVO HIP COMPONENTS

FDA UDI
Synovo Production·00814193025821·HIP ACETABULAR FIXATION CUP - 58 MM 5 HOLE

B-P TOTAL HIP SYSTEM

FDA UDI
ENDOTEC, INC.·00814193022639·B-P HIP ACETABULAR FIXATION CUP W/BIOCOAT & W/U...

SENSITITRE 18-24 HOURS SUSCEPTIBILITY PLATES (QUINUPRISTIN/DALFOPRISTIN)

FDA 510(k)
FDA Class 2 ·Microbiology

SYNTHES (USA) WRIST FUSION PLATES (WFP)

FDA 510(k)
FDA Class 2 ·Orthopedic

QUANTA SYSTEM S.P.A.

FDA Adverse Event
Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·December 21, 2012

COAPTITE INJECTABLE IMPLANT

FDA Adverse Event
Other ·MERZ AESTHETICS, INC.·Product code LNM·November 4, 2011

COAPTITE INJECTABLE IMPLANT

FDA Adverse Event
Other ·BIOFORM MEDICAL, INC.·Product code LNM·July 2, 2010

PORTEX ENDOTRACHEAL TUBE, SILICONIZED

FDA Adverse Event
Malfunction ·SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.·Product code BTR·May 13, 2025

FOX PLUS PTA CATHETER

FDA Adverse Event
Injury ·ABBOTT VASCULAR SWITZERLAND·Product code LIT·October 2, 2008

DEXTRUS 4137

FDA Adverse Event
Death ·BIOTRONIK SE & CO. KG·Product code NVN·March 19, 2013

INTERSTIM

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·March 1, 2011