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

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TEM 3000 HEAD COIL

FDA 510(k)
FDA Class 2 ·Radiology

York 4 Trolley

FDA UDI
FERNO-WASHINGTON, INC.·00190790000455·York 4 Trolley, ship w/wheels off

econom® Vac. 2.7 V / XL 2.5 V,

FDA UDI
Rudolf Riester GmbH·04045396130593·The Riester otoscope is produced for illuminati...

JOBST forMen

FDA UDI
BSN MEDICAL, INC.·04042809849936·FOR MEN 15-20 MM HG KNEE HIGH OPEN TOE SMALL NA...

Mariner Outrigger

FDA UDI
Seaspine Orthopedics Corporation·10889981173890·L Con, Side-Loading, R, 16mm, 200mm

CAPELLA

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

1.5T INFINITY TWINSPEED MR SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

NUVASIVE

FDA Adverse Event
Injury ·NUVASIVE·Product code NKB·January 10, 2011

ARCHITECT CA19-9XR

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code NIG·October 31, 2025

ALINITY I CA 19-9XR REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code NIG·May 19, 2026

ACTIVA

FDA Adverse Event
Injury ·NEURO - VILLALBA·Product code MHY·April 11, 2013

XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code NIQ·April 12, 2011

FLORENCE BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL QUEBEC, LP·Product code FNL·May 21, 2008

ALINITY I CA 19-9XR REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code NIG·May 1, 2026

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

ALINITY I CA 19-9XR REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code NIG·May 14, 2026

ALINITY I CA 19-9XR REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code NIG·December 9, 2025

ARCHITECT CA19-9XR

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code NIG·December 22, 2025

ARCHITECT CA19-9XR

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code NIG·April 3, 2026

ALINITY I CA 19-9XR REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code NIG·November 4, 2025