9 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFICATION TO ASTRA TECH IMPLANT - DENTAL SYSTEM
FDA 510(k)
FDA Class 2
·Dental
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690189374·AK3 Femoral Distal Locating Device, 4° Bushing
MSI
FDA UDI
Modern Surgical Instruments LLC·00810130203703·Round handle micro cervical curette 10", bwd an...
MSI
FDA UDI
Modern Surgical Instruments LLC·B419MSI9903040·
Kingon P2 Oxygen Concentrator
FDA 510(k)
FDA Class 2
·Anesthesiology
WAVEON WRX BONE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·March 5, 2013
CAPSURE SENSE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 7, 2014