16 results · 30ms · 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.

780 nm L11 LED Light Source with AIM

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

TALOS® HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167322216110·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676221611000·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167312216110·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676221611070·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676221611150·

QAB2A IGG ELISA KIT HRP

FDA 510(k)
FDA Class 2 ·Immunology

AMPLATZER TORQVUE FX

FDA 510(k)
FDA Class 2 ·Cardiovascular

Unison®-C Anterior Cervical Fixation System

FDA UDI
Pioneer Surgical Technology, Inc.·00846468083335·Interbody Fusion Device, 22mm (W), 16mm (D), 11...

Unison®-C Anterior Cervical Fixation System

FDA UDI
Pioneer Surgical Technology, Inc.·00846468083403·Interbody Fusion Device, 22mm (W), 16mm (D), 11...

Unison®-C Anterior Cervical Fixation System

FDA UDI
Pioneer Surgical Technology, Inc.·00846468081720·Trial, 22mm (W), 16mm (D), 11mm (H), 7° Lordosis

PREFACE® GUIDING SHEATH WITH MULTIPURPOSE CURVE

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DYB·November 3, 2014

LOCKING SCREW, FULLY THREADED 5X30 MM

FDA Adverse Event
Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·August 19, 2011

INTELLIVUE TELEMETRY SYSTEM

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·July 1, 2013

Unison®-C Anterior Cervical Fixation System

FDA UDI
Pioneer Surgical Technology, Inc.·00846468082284·Rasping Trial, 22mm (W), 16mm (D), 11mm (H), 7°...

Model Number L111, ESSENTIO DR SL MRI Pacemaker

FDA Enforcement
Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025