26 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ELIBRA SOFT-TISSUE FORCE SENSOR
FDA 510(k)
FDA Class 2
·Neurology
Peerless Buccal Tube
FDA UDI
ORMCO CORPORATION·00889989053463·PEERLESS 2NDMOL 6DEG LR WDX-20TX018
NexxZr™ T / D-100-18-NT-C100-SD
FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271113146·
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981204587·Trial, 11mm x 32mm x 10mm, 5 Deg
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981190439·Interbody, 11mm x 32mm x 10mm, 5 Deg
WaveForm TO
FDA UDI
Seaspine Orthopedics Corporation·10889981288778·Interbody, 11mm x 32mm x 10mm, 5 Deg, 3D
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361037125·SLIM GUIDE, SLIM PEEK INSERTER - 9MM
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361037156·SLIM GUIDE, SLIM PEEK INSERTER - 12MM
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361037118·SLIM GUIDE, SLIM PEEK INSERTER - 8MM
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361037149·SLIM GUIDE, SLIM PEEK INSERTER - 11MM
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361037088·SLIM GUIDE, SLIM PEEK INSERTER - 5MM
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361037132·SLIM GUIDE, SLIM PEEK INSERTER - 10MM
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361037101·SLIM GUIDE, SLIM PEEK INSERTER - 7MM
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361037095·SLIM GUIDE, SLIM PEEK INSERTER - 6MM
GE VIVID P3 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
AMNIOLENS
FDA 510(k)
FDA Class 2
·Ophthalmic
RAVINE Lateral Access System
FDA UDI
VB Spine LLC·10888857560918·A/P Lateral Access Blade Size 13x100 mm
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·April 5, 2000
ADVANCE 35 LP LOW PROFILE BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·February 3, 2017
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 1, 2014