25 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Chiavaye Personal Moisturizer
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Valence Robotic Navigation System
FDA UDI
ALPHATEC SPINE, INC.·00190376681122·Registration Adapter
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167312510110·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167322510110·
ihc Enhancer Kit, 30mL
FDA UDI
NOVODIAX, INC.·00850000596528·
PLIF Cage
FDA UDI
Eisertech, LLC·B523100097251011·PLIF CAGE, LORDOTIC, 25AP X 10ML X 11HT
ihc Enhancer Kit, 15mL
FDA UDI
NOVODIAX, INC.·00850000596511·
ihc Enhancer 5mL
FDA UDI
NOVODIAX, INC.·00850030934598·
FPS
FDA UDI
Tyber Medical, LLC·00810040686047·Ø2.5mm Non-locking Screw, 11mm
PLIF Cage
FDA UDI
Eisertech, LLC·B523100035251011·PLIF CAGE, NON-LORDOTIC, 25AP X 10ML X 11HT
ihc Enhancer 15mL
FDA UDI
NOVODIAX, INC.·00850030934604·
RUNTHROUGH GUIDE WIRE FOR CARDIAC CATH
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 26, 2024
RUNTHROUGH NS
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 9, 2017
ENDOSSEOUS DENTAL IMPLANT ABUTMENT
FDA 510(k)
FDA Class 2
·Dental
VISERA 4K UHD SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ELMED
FDA UDI
ELMED INCORPORATED·00842180163546·4MM, 45CM, NEW CATHETER PASSER, SHUNT GUIDE W/ ...
LINOX SD 65/18
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code LWS·September 12, 2011
PROTEGE
FDA Adverse Event
Death
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 29, 2013
BD MICROLANCE¿ 3 HYPODERMIC NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·December 12, 2018