8 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SUNGLASSES
FDA 510(k)
FDA Class 1
·Ophthalmic
MCCUE PLC ENERGIST ULTRA VARIABLE PULSED LIGHT SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
COROENT THORACOLUMBAR IMPLANTS
FDA 510(k)
FDA Class 2
·Orthopedic
LAMITRODE 44C LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION DIV·Product code LGW·December 22, 2010
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 29, 2013
RECAP PF FMRL HD RESURF 52MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KXA·July 17, 2014
NASAL-AIRE
FDA Adverse Event
Malfunction
·INNOMED TECHNOLOGIES·Product code BYE·January 6, 2003
EVOLUT FX DCS
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NPT·November 10, 2025