859 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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4MP COLOR LCD MONITOR, RADIFORCE RX440
FDA 510(k)
FDA Class 2
·Radiology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694003353·2 x 2 x 2 L Plate
8.0 X 130mm Cann Screw Fastener 70mm Var Thd
FDA UDI
Osteocentric Technologies, Inc.·00810074306881·8.0 X 130mm Cann Screw Fastener 70mm Var Thd
Ø7.0 x 70mm x 130mm CANNULATED PARTIAL THREAD SCREW
FDA UDI
Osteocentric Technologies, Inc.·00816950027086·Ø7.0 x 70mm x 130mm CANNULATED PARTIAL THREAD S...
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981175764·Z-Rod, Dia. 6.0mm, Titanium, 70mm
GPS TM, G SURGICAL ANTERIOR CERVICAL PLATE SYSTEM +
FDA 510(k)
FDA Class 2
·Orthopedic
UNIPLATE ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Widex
FDA UDI
Widex A/S·05706069575637·Widex UNIQUE U-FM (Copper brown ) 330, RC coil
Widex
FDA UDI
Widex A/S·05706069553659·Widex UNIQUE U-FA (Copper brown ) 330, Telecoil...
Widex
FDA UDI
Widex A/S·05706069556346·Widex D-FA P (Copper brown ) Dream 330, Telecoi...
Widex
FDA UDI
Widex A/S·05706069564129·Widex UNIQUE U-FP (Copper brown ) 330, Telecoil...
GREENLIGHT MOXY FIBER OPTIC
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·May 20, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code CAW·September 30, 2014
ENPULSE
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DXY·June 16, 2011
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 14, 2026
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026