416 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IPS E.MAX PRESS MULTI
FDA 510(k)
FDA Class 2
·Dental
ARGELOY NP SUPREME 25kg
FDA UDI
ARGEN CORPORATION, THE·D818120134·Base metal alloy
OsteoMed
FDA UDI
OSTEOMED LLC·00845694002738·Square Plate
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319703410·Adson Tissue Forceps 4-3/4" (11.9cm), 1x2 teeth...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197539883·Spurling Laminectomy Ronguer downwards a
ngled ...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197030861·Cooley Vascular scissor 18,4cm long
curved...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197030878·Cooley Vascular scissor 23.0cm long
curved...
SPIRAL RADIUS 90-D RODDING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MODEL LA-1200 MULTI-CHANNEL LASER THERAPY SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
PRECISE SDS SELF EXPANDING
FDA Adverse Event
Death
·CORDIS DE MEXICO·Product code FGE·November 21, 2012
PRECISE SDS SELF EXPANDING
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code FGE·November 21, 2012
PRECISE SDS SELF EXPANDING
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code FGE·November 21, 2012
PRECISE SDS SELF EXPANDING
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code FGE·November 21, 2012
PRECISE SDS SELF EXPANDING
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code FGE·November 21, 2012
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 20, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 25, 2014
SHILEY
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code JOH·June 3, 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