66 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NOVEL SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Theragenics
FDA UDI
THERAGENICS CORPORATION·00813787021867·
Mick 5mm gold fiduciary marker,18G, 3 pack (30pc)
FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330021786·
Rebar
FDA UDI
Micro Therapeutics, Inc.·00836462002197·MICRO CATH 105-5081-153 REBAR IR
Rebar
FDA UDI
Micro Therapeutics, Inc.·00763000412487·MICRO CATH 105-5081-153 V05 REBAR
Rebar
FDA UDI
Micro Therapeutics, Inc.·00763000539344·MICRO CATHETER 105-5081-153 V08 SMB
RebarTM
FDA UDI
Micro Therapeutics, Inc.·00847536026834·MICRO CATH 105-5081-153 V01 REBAR
ALANTE, BATTERY OPERATED POWER WHEELCHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
MODIFICATION TO STEATHSTATION TREATMENT GUIDANCE PLATFORM
FDA 510(k)
FDA Class 2
·Neurology
WAVEWRITER ALPHA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 11, 2024
SOLITAIRE FR4
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·July 16, 2025
REBAR
FDA Adverse Event
Malfunction
·MEDTRONIC DOMINICANA·Product code KRA·April 11, 2025
SOLITAIRE FR
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·April 21, 2025
REBAR
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code KRA·June 21, 2017
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·April 26, 2013
COOL PATH DUO 7F, 1304-CP2-7-1.5(5)-L1-TE4BE1AB
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, IRVINE·Product code OAD·April 14, 2011
EVEREST BIPOLAR BICOAG LP SCISSORS
FDA Adverse Event
Malfunction
·GYRUS MEDICAL, INC·Product code GEI·July 15, 2008
REBAR
FDA Adverse Event
Malfunction
·MEDTRONIC DOMINICANA·Product code KRA·March 26, 2025
UNKNOWN SOLITAIRE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·June 27, 2024
REBAR
FDA Adverse Event
Malfunction
·MEDTRONIC DOMINICANA·Product code KRA·May 16, 2025