66 results · 23ms · Sources: EU EUDAMED, 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