34 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TROCHANTERIC NAIL
FDA 510(k)
FDA Class 2
·Orthopedic
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890107801·Zirlux Guide Pin
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450249802·
TiWAVE L Lumbar Cage System
FDA UDI
Kalitec Direct LLC·B07323K0107000·Tamp, Advancing
NINE WEST
FDA UDI
FGX INTERNATIONAL INC.·00193033237908·
NINE WEST
FDA UDI
FGX INTERNATIONAL INC.·00193033237892·
NINE WEST
FDA UDI
FGX INTERNATIONAL INC.·00193033237915·
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345023789·Straight Tamp
NINE WEST
FDA UDI
FGX INTERNATIONAL INC.·00193033237922·
SYMPHONY
FDA Adverse Event
Injury
·SORIN CRM·Product code NVZ·September 24, 2010
INSTANT-VIEW MORPHINE (2000) URINE CASSETTE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
COPAN VIRAL TRANSYSTEM
FDA 510(k)
FDA Class 1
·Microbiology
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 30, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026
PLASMABLADE ADENOID TIP
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·March 19, 2013
EON MINI RECHARGEABLE IPG
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·March 2, 2011
ATLAS II VR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024