44 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CUPID Brand Male Natural Rubber Latex Condoms (Plain (banana) , Plain (strawberry), Dotted , Multi-textured (Dotted+Contoured + Ribbed))
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
HHM
FDA UDI
Oticon A/S·05707131356079·G500 S, MINIRITE R LI-ION 2.4G C094 HHM
Ophthlamic Speculum
FDA UDI
KATENA PRODUCTS, INC.·10841668115159·BARRAQUER SPECULUM Disposable with Finger tabs ...
Ophthlamic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668115541·INFANT SPECULUM 4MM SOLID (10/BX)
Apelo® / Apelo® MIS
FDA UDI
ATLAS SPINE, INC.·M68120106700000·MIS Cannulated Screwdriver
DADE BEHRING COAGULATION ANALYZER (BCT)
FDA 510(k)
FDA Class 2
·Hematology
SURESIGNS VM4, SURESIGNS VM6, SURESIGNS VM8 MODEL: 863063, 863064, 863065, 863066, 863068
FDA 510(k)
FDA Class 2
·Cardiovascular
BELLAFILL DERMAL FILLER
FDA Adverse Event
Injury
·TIGER AESTHETICS MEDICAL LLC·Product code LMH·September 19, 2025
WINGSPAN STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code NJE·December 2, 2010
WINGSPAN STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code NJE·December 2, 2010
WINGSPAN STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code NJE·December 2, 2010
WINGSPAN STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code NJE·December 3, 2010
ABGII MODULAR LONG NECK
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CORK·Product code MEH·January 13, 2014
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·October 27, 2014
BREEZE2
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·July 1, 2011
ULTRAPRO MESH
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·July 2, 2013
WINGSPAN STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code NJE·December 2, 2010
UNKNOWN DEEP BRAIN STIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·February 16, 2011
WINGSPAN STENT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT·Product code NJE·December 3, 2010
UNKNOWN DEEP BRAIN STIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·February 17, 2011