26 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CRIT-LINE MONITOR III TQA (CLM TQA)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040011553·Zirlux 16+ 0M1 95X14
QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 12, 2026
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033337301·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033337332·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033337349·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033337295·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033337356·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112410·Awl Tap, 4.5 mm, Fixed Sleeve
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033337325·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033337318·
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 9, 2025
WATERLASE, MILLENNIUM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RADIONICS RF DISC CATHETER ELECTRODE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PRECISION MONTAGE MRI
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 13, 2019
PERCLOSE¿ PROSTYLE¿
FDA Adverse Event
Injury
·ABBOTT VASCULAR INC.·Product code MGB·October 3, 2025
PERCLOSE¿ PROSTYLE¿
FDA Adverse Event
Injury
·ABBOTT VASCULAR INC.·Product code MGB·October 3, 2025
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·March 19, 2013
OPUS MAGNUM2 IMPLANT KNOTLESS FIXATION DEVICE
FDA Adverse Event
Other
·ARTHROCARE CORP·Product code MBI·March 3, 2011
ACCU-CHEK COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 11, 2008