42 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NUMARIS 4VA15A
FDA 510(k)
FDA Class 2
·Radiology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040019092·Zirlux 16+ 20x19x15 C1
uni® I otoscope XL 3.5 V, plug-in-style
FDA UDI
Rudolf Riester GmbH·04045396130135·The Riester otoscope is produced for illuminati...
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0112020·Tap, 4.75mm
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033402146·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033402115·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033402122·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033402139·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033402092·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033402108·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033403327·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033402153·
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026
KARMAN WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
OWL RADIOFREQUENCY SYSTEM, MODEL URF-2A, AND ASSOCIATE RADIOFREQUENCY LESION PROBES
FDA 510(k)
FDA Class 2
·Neurology
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·December 22, 2025
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC,USA·Product code LFR·May 16, 2007
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 13, 2013
DIAGNOST 93
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code JAA·February 1, 2011