17 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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A.B. DENTAL DEVICES DENTAL IMPLANTS SYSTEM
FDA 510(k)
FDA Class 2
·Dental
NexxZr™ T / D-100-16-NT-C300-SD
FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271113351·
Clear Readers
FDA UDI
Diversified Products, Inc.·00037741113218·
Reef TH
FDA UDI
Seaspine Orthopedics Corporation·10889981200817·Interbody, 11mm x 32mm x 12mm, 15 deg
MAYO-HEGAR NEEDLE HOLDER
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896021891·MAYO-HEGAR NEEDLE HOLDER TUNGSTEN CARBIDE SERRA...
WaveForm TO
FDA UDI
Seaspine Orthopedics Corporation·10889981288839·Interbody, 11mm x 32mm x 12mm, 15 Deg, 3D
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981204662·Trial, 11mm x 32mm x 12mm, 15 Deg
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981190514·Interbody, 11mm x 32mm x 12mm, 15 Deg
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981207939·Trial, 11mm x 32mm x 12mm, 15 deg
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981192822·Interbody, 11mm x 32mm x 12mm, 15 deg
Clear Readers
FDA UDI
Diversified Products, Inc.·00842894113875·
CSTAT, MODELS 09-0014-01 AND 09-0014-02
FDA 510(k)
FDA Class 2
·Cardiovascular
PATIENT-SPECIFIC VANGUARD FEMORAL COMPONETS
FDA 510(k)
FDA Class 2
·Orthopedic
12/14 ARTICUL 40MM M SPEC+1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 29, 2013
COULTER AC*T DIFF 2 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·June 17, 2011
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·August 21, 2008
TRUE METRIX
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH INC·Product code NBW·May 26, 2022