360 results · 33ms · 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.

REVOLUTION SPINAL FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

S4 IMPLANTS

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code KWP·August 29, 2008

Baltic Denture System BD Load

FDA UDI
Merz Dental GmbH·D7091032219·Baltic Denture System BDLoad ↓ Mm6 PLSEum2DFm A...

Battalion

FDA UDI
ALPHATEC SPINE, INC.·00840967187679·Battalion, LLIF Trial, 15°, 22 mm Wide, 19 mm X...

WANDY SELF-ADHESIVE NEUROSTIMULATION ELECTRODE

FDA 510(k)
FDA Class 2 ·Neurology

SCALPFIX CLIP SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·April 3, 2013

SPHINCTEROTOME

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FDI·March 29, 2011

LOGICAL 60" SINGLE LINE MONITORING KIT

FDA Adverse Event
Malfunction ·SMITHS MEDICAL, ASD·Product code DRS·April 18, 2008

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

SCP PANEL CENTRIFUGE JMS

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·November 5, 2013

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 20, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025