1,764 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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RESTORATION ADM SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PMMA disc
FDA UDI
Dentsply International Inc.·D00180720200·
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108692402·Conical Angulated 20 Deg knife edge Ti Abutment
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0120200·Tower Tab Slider, MIS
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0120200·Screwdriver, Modular Bone Screws
InSePtion MIS Fixation System
FDA UDI
Kalitec Direct LLC·B07314K0120200·Inserter, Locking Plate
Optimus Q
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215058258·
Arsenal
FDA UDI
ALPHATEC SPINE, INC.·00844856084360·POLYAXIAL SCREW, 7.2mm X 20mm
Arsenal
FDA UDI
ALPHATEC SPINE, INC.·00844856086692·POLYAXIAL REDUCTION SCREW, 7.2mm X 20mm
Arsenal
FDA UDI
ALPHATEC SPINE, INC.·00844856085510·SACRAL POLYAXIAL SCREW, 7.2mm X 20mm
Arsenal
FDA UDI
ALPHATEC SPINE, INC.·00190376074054·Polyaxial Screw, 7.2 mm x 20 mm
Genius Total Knee System
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215022976·
Arsenal
FDA UDI
ALPHATEC SPINE, INC.·00190376077512·Polyaxial Reduction Screw, 7.2 mm x 20 mm
LACTOSORB MENISCAL SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
RESPIEVENTS SOFTWARE IS EVENT DATA PROCESSING SOFWARE FOR A PC
FDA 510(k)
FDA Class 2
·Cardiovascular
AED PRO
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·April 20, 2011
UNKNOWN_NEUROVASCULAR_PRODUCT
FDA Adverse Event
Death
·STRYKER NEUROVASCULAR CORK·Product code NJE·April 22, 2013
CAPSURE SP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 17, 2020
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·November 2, 2020