10,000 results
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55ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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X-SMART IQ MEASUREMENT CABLE
FDA Adverse Event
Malfunction
·MAILLEFER INSTRUMENTS HOLDING SARL·Product code LQY·September 23, 2020
X-SMART IQ BASIC STARTER KIT
FDA Adverse Event
Malfunction
·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EBW·September 28, 2022
PROPEX IQ APEX LOCATOR
FDA Adverse Event
Malfunction
·DENTSPLY MAILLEFER·Product code LQY·July 14, 2021
PROPEX IQ APEX LOCATOR
FDA Adverse Event
Malfunction
·DENTSPLY MAILLEFER·Product code LQY·September 3, 2020
GE Healthcare Discovery IQ X-ray system
FDA Enforcement
Class II
·Terminated·GE Healthcare, LLC·June 21, 2017
GE Healthcare Discovery IQ X-ray system
FDA Recall
Terminated
·GE Healthcare, LLC·Product code KPS·May 19, 2017
TRULIANT KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·November 11, 2024
Omega IV and Omega V tables on GE Innova 4100/4100IQ GE Innova 4100 / 4100 IQ., x-ray system
FDA Recall
Terminated
·GE Medical Systems, LLC·Product code MQB·December 22, 2009
Hook, External Limb Component, Mechanical
FDA classification
FDA Class 1
·Hook, External Limb Component, Mechanical
HQX
FDA UDI
TOP-RANK HEALTH CARE CO., LTD.·06973602730078·
HQX
FDA UDI
TOP-RANK HEALTH CARE CO., LTD.·06973602730061·
IOX CO. LTD.
FDA registration
IOX CO. LTD.·3 products·🇯🇵 Japan
MolecuLight i:X
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MolecuLight I:X
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MolecuLight I:X
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MolecuLight i:X
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
IDx-DR
FDA UDI
Digital Diagnostics Inc.·00860005195626·
IDx-DR
FDA UDI
Digital Diagnostics Inc.·00860005195619·
Taper-Lock™
FDA UDI
ZimVie US Corp LLC·00889024015531·
Invacare® AVIVA FX Power Wheelchair
FDA UDI
INVACARE CORPORATION·00841447111658·Invacare® AVIVA FX Power Wheelchair