297 results
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40ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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COMPASS
FDA 510(k)
FDA Class 2
·Ophthalmic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699526·GENUMEDI PSS BLUE, SIZE O
CoRoent
FDA UDI
Nuvasive, Inc.·00887517577665·CoRoent Ant TLIF PEEK, 15x10x32mm 0°
DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169523937·TRIAL 2150320 PLATE TRIAL 20MM
TiLock
FDA UDI
Genesys Orthopedics Systems LLC·M719G1503200·Pre-Bent Rod
FREESCAN LATEX-FREE ULTRASOUND TRANSDUCER COVER KIT
FDA 510(k)
FDA Class 2
·Radiology
SLENDERTONE SYSTEM ULTRA MODEL E70/X70
FDA 510(k)
FDA Class 2
·Physical Medicine
Widex
FDA UDI
Widex A/S·05706069887303·WIDEX MOMENT M-IP (Dark brown ) 220, Left
Widex
FDA UDI
Widex A/S·05706069887297·WIDEX MOMENT M-IP (Clay brown ) 220, Left
Widex
FDA UDI
Widex A/S·05706069887280·WIDEX MOMENT M-IP (Light beige ) 220, Left
Widex
FDA UDI
Widex A/S·05706069819779·Widex UNIQUE U-IP (Light beige ) 220, Left
Widex
FDA UDI
Widex A/S·05706069819793·Widex UNIQUE U-IP (Dark brown ) 220, Left
Widex
FDA UDI
Widex A/S·05706069819786·Widex UNIQUE U-IP (Clay brown ) 220, Left
530G INSULIN PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 7, 2014
6.0MM TI CURVED SOFT ROD 70MM
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code NKB·June 6, 2013
MINICAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 6, 2011
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026