416 results · 25ms · Sources: EU EUDAMED, 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