26 results · 21ms · Sources: EU EUDAMED, US FDA

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Sonata Transcervical Fibroid Ablation System 2.2

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

CoRoent

FDA UDI
Nuvasive, Inc.·00887517569851·CoRoent Ant TLIF Ti, 12x12x30mm 4°

Sonic

FDA UDI
Sonic Innovations, Inc.·05714464007165·SONIC RADIANT 80 MNR T R BL DEMO

HEALIX ADVANCE ORTHOCORD

FDA UDI
Medos International Sàrl·10886705021406·HEALIX ADVANCE PEEK 3 SUTURE ANCHOR w/ORTHOCORD...

LEONE SPA

FDA UDI
LEONE SPA·08033707040118·DB BRACKETS MINI 22 CUS

CONAIR LLC.

FDA registration
CONAIR LLC.·12 products·🇺🇸 United States

HUMAN C1 INACTIVATOR KIT FOR USE ON SPAPLUS

FDA 510(k)
FDA Class 2 ·Immunology

ACCUMAP AUTOMATIC PERIMETER

FDA 510(k)
FDA Class 2 ·Neurology

1222304-2016-00015

FDA Adverse Event
Injury ·February 26, 2016

CONAIR

FDA Adverse Event
Malfunction ·CONAIR LLC.·Product code IRT·May 30, 2025

CONAIR

FDA Adverse Event
Injury ·CONAIR CORPORATION·Product code IRT·March 1, 2017

CONAIR

FDA Adverse Event
Injury ·CONAIR CORPORATION·Product code IRT·March 1, 2017

CONAIR

FDA Adverse Event
Malfunction ·CONAIR CORPORATION·Product code IRT·April 20, 2016

Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

FDA Enforcement
Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 18, 2026

CONAIR

FDA Adverse Event
Injury ·CONAIR CORPORATION·Product code IRT·March 1, 2016

CONAIR

FDA Adverse Event
Malfunction ·CONAIR CORPORATION·Product code IRT·April 28, 2017

CONAIR

FDA Adverse Event
Injury ·CONAIR CORPORATION·Product code IRT·December 21, 2016

PINNACLE MTL INS NEUT36IDX50OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 3, 2014

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 24, 2011

STEALTHSTATION S7 SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·July 12, 2013