7 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OPTUS SINUSCOPES AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
FLOWERS NASAL IMPLANT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OHMEDA DOUBLE SWIVEL ADAPTER
FDA 510(k)
FDA Class 1
·Anesthesiology
PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES
FDA Adverse Event
Malfunction
·INVACARE SUZHOU·Product code BTI·February 5, 2013
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·January 3, 2011
OMNILINK ELITE PERIPHERAL STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIO·July 18, 2014
OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·October 13, 2021