28 results · 25ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

IMMULITE HOMOCYSTEINE MODEL LKHO1 / IMMULITE 2000 HOMOCYSTEINE MODEL L2KHO2

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

KALORE™

FDA UDI
Gc America Inc.·14548161293310·KALORE™ Syringes (2 mL/4 g) CVT

KALORE™

FDA UDI
Gc America Inc.·D0470035971·KALORE™ Syringes (2 mL/4 g) CVT

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756134026·Custom Anesthesia Circuit

VITA RESPONSE

FDA 510(k)
FDA Class 2 ·Dental

CONMED TROGARD FINESSE TROCAR SYSTEM, MODEL 60-6050-XXX

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

SYRINGE 30ML LL S/C 56

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·March 27, 2025

SYRINGE 30ML LL S/C 56

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·March 26, 2025

SYRINGE 30ML LL S/C 56

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·March 26, 2025

WAVEWRITER ALPHA?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 12, 2025

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 2, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

CLEARGLIDE EVH LONGVIEW W/SCIS

FDA Adverse Event
Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 23, 2009

CLEARGLIDE EVH SMALL

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

CLEARGLIDE EVH SMALL W/SCISSOR

FDA Adverse Event
Malfunction ·SORIN GROUP USA, INC.·Product code GEI·October 16, 2009

CLEARGLIDE EVH LONGVIEW W/SCIS

FDA Adverse Event
Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 9, 2009

VERSACARE BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·February 11, 2013