18 results · 24ms · Sources: EU EUDAMED, US FDA

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EkoSonic Endovascular Device, EKOS+ Endovascular Device

FDA 510(k)
FDA Class 2 ·Cardiovascular

NA

FDA UDI
SYNTHES (U.S.A.) LP·10886982153241·5.0MM LOCKING SCREW SELF-DRILLING 22MM

Prime Medical LLC

FDA UDI
Prime Medical LLC·00850055249271·PrimePadPlus-K12-3422

Prime Medical LLC

FDA UDI
Prime Medical LLC·00850055249257·PrimePadPlus-K1-3422

Prime Medical LLC

FDA UDI
Prime Medical LLC·00850055249264·PrimePadPlus-K2-3422

CARDIQ FUNCTION

FDA 510(k)
FDA Class 2 ·Radiology

TERUMO SURGUARD 3 SAFETY NEEDLE TERUMO SURGUARD 3 HYPODERMIC SYRINGE WITH SAFETY NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

JDEVOLUTION PLUS

FDA Adverse Event
Injury ·J DENTAL CARE SRL·Product code DZE·August 6, 2025

JDEVOLUTION PLUS

FDA Adverse Event
Injury ·J DENTAL CARE SRL·Product code DZE·August 6, 2025

INRATIO PT/INR TEST STRIPS

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·October 23, 2014

ASR UNI FEMORAL IMPL SIZE 45

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 12, 2011

LIFEPAK(R) 1000 DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 9, 2013

NEEDLE, HYPODERMIC, SINGLE LUMEN

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·September 1, 2020

TERUMO SURGUARD3 SAFETY HYPODERMIC NEEDLE

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·August 28, 2018

NEEDLE, HYPODERMIC, SINGLE LUMEN

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·November 8, 2019

TERUMO SURGUARD3 SAFETY HYPODERMIC NEEDLE

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·November 13, 2018

SURGUARD3 SAFETY HYPODERMIC NEEDLE

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·December 6, 2024

TERUMO SURGUARD3 SAFETY HYPODERMIC NEEDLE

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·December 2, 2022