50 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ENSITE ARRAY MULTI-ELECTRODE DIAGNOSTIC CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Invictus
FDA UDI
ALPHATEC SPINE, INC.·00190376240985·AO Quick Connect Axial Handle, Fixed with Jewel...
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311210060·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321210060·
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117810·Stemmed Modular Tibia Tray Trial Size 6
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450383704·
STARTOX DRUG OF ABUSE SCREENING TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
VANISH POINT INSULIN SYRINGES 1CC - 29G X 1/2"
FDA Adverse Event
Malfunction
·RETRACTABLE TECHNOLO...·Product code FMF·September 19, 2013
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469174·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469150·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469204·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469167·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469181·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469136·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469198·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024469143·
ARTEFILL DERMAL FILLER
FDA Adverse Event
Injury
·SUNEVA MEDICAL, INC.·Product code LMH·April 13, 2018
CUSTOM PROXIMAL FEMUR IMPLANT
FDA Adverse Event
Malfunction
·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 23, 2014
CUSTOMER PROXIMAL FEMUR REPLACEMENT IMPLANT
FDA Adverse Event
Injury
·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 19, 2014