26 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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