17 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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V10
FDA 510(k)
FDA Class 2
·Cardiovascular
QUANTUM IM COMPOSITE NAILING SYSTEM (QUANTUM NAILING SYSTEM)
FDA 510(k)
FDA Class 2
·Orthopedic
PASS LP SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
GLIDEWIRE GT
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 30, 2026
ENTERRA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LNQ·October 14, 2014
POWERED WHEELCHAIR
FDA Adverse Event
Injury
·INVACARE TAYLOR STREET·Product code ITI·July 21, 2011
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 24, 2013
GLIDEWIRE GT
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2026
CARTO VIZIGO 8.5F BI-DIRECTIONAL GUIDING SHEATH - MEDIUM
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code DYB·August 31, 2021
GALAXY G3 MINI 2MM X 3CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·May 18, 2022
CASH 14 PLAT COIL 4MMX6CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·May 18, 2022
GALAXY G3 MINI 2MM X 3CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·May 18, 2022
CARTO VIZIGO 8.5F BI-DIRECTIONAL GUIDING SHEATH - MEDIUM
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code DYB·June 8, 2021
RADIFOCUS GLIDEWIRE
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 26, 2025
TERUMO RADIFOCUS GUIDE WIRE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 3, 2025
GLIDEWIRE GT
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 21, 2018
GALAXY G3 MINI 3MM X 6CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·May 18, 2022