26 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LYRA G SERIES SURGICAL LASER SYSTEM (SL SERIES Q-SWITCHED ND:YAG CONFIGURATION)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526743557·LEVAMED ANKLE SUPPORT SILVER IV
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033125281·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033125304·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033125250·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033354537·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033125267·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033125274·
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345023970·PADDLE SPREADER, 14MM
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0102140·Shaver, Open 14mm
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033125243·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033125298·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033354551·
ORTHOSORB ABSORBABLE
FDA Adverse Event
Injury
·JOHNSON & JOHNSON PROFESSIONAL, INC.·Product code MBJ·December 10, 1996
STEALTHSTATION SYSTEM GOLDENEYE MICRO-MAGNETIC TRACKING SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
REAL PATIENT REAL PATIENT 128 CHANNEL EEG HEADBOX, MODEL EX-NW-128-RP
FDA 510(k)
FDA Class 2
·Neurology
BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 16, 2023
RUBY COIL
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code HCG·October 8, 2015
AMPLATZ SUPER STIFF GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code DQX·March 19, 2013
PORTEX 8.5 CUFFED TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL LTD.·Product code JOH·February 11, 2011