16 results
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36ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NEUROPTICS, INC.
FDA registration
NEUROPTICS, INC.·1 product·🇺🇸 United States
NeurOptics
FDA UDI
Neuroptics, Inc.·00850010118123·
NeurOptics
FDA UDI
Neuroptics, Inc.·10850010118038·Box of 24 Smart Guards
NeurOptics
FDA UDI
Neuroptics, Inc.·00850010118109·
NeurOptics
FDA UDI
Neuroptics, Inc.·00850010118079·
NeurOptics
FDA UDI
Neuroptics, Inc.·00850010118093·
NeurOptics
FDA UDI
Neuroptics, Inc.·00850010118024·
NeurOptics
FDA UDI
Neuroptics, Inc.·00850010118000·
NeurOptics
FDA UDI
Neuroptics, Inc.·00850010118017·
NeurOptics
FDA UDI
Neuroptics, Inc.·00850010118086·
NeurOptics
FDA UDI
Neuroptics, Inc.·00850010118116·
NPI 200
FDA Adverse Event
Malfunction
·NEUROPTICS INC.·Product code HLG·October 4, 2017
NEUROPTICS
FDA Adverse Event
Malfunction
·NEUROPTICS, INC.·Product code HLG·April 16, 2021
PUPILLOMETER
FDA Adverse Event
Injury
·NEUROPTICS, INC.·Product code HLG·January 16, 2024
LAMITRODE TRIPPLE LEAD 16C, 60 CM LENGTH
FDA Adverse Event
Injury
·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 17, 2008
EON 16-CHANNEL IPG
FDA Adverse Event
Injury
·ADVANCED NEUROMODULATION SYSTEMS INC.·Product code LGW·September 17, 2008