7 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Electric Wheelchair
FDA 510(k)
FDA Class 2
·Physical Medicine
K-Y BRAND ULTRA GEL PERSONAL LUBRICANT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ONE TOUCH ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·October 30, 2008
PRECISE PRO RX CAROTID STENT SYSTEM
FDA Adverse Event
Death
·CORDIS DE MEXICO·Product code NIM·August 23, 2011
SECURESTRAP 5MM ABSORBABLE STRAP FIXATION DEVICE
FDA Adverse Event
Injury
·ETHICON INC.·Product code GDW·July 11, 2013
Model Number L111, ESSENTIO DR SL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025