9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
DUNLAP HEAT PAD
FDA 510(k)
FDA Class 2
·Physical Medicine
REVELATION DIAMOND
FDA UDI
Ss White Burs, Inc.·D6909111952·REVELATION DIAMOND 859-016F - 5 PACK
PRIZM BLADE (MORIA MODEL) LSK / MK8510LSK; PRIZM BLADE (MORIA MODEL) CB / MK8511CB
FDA 510(k)
FDA Class 1
·Ophthalmic
VALUTRUS REUSABLE CIRCULAR STAPLER AND DISPOSABLE RELOADS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
QUICK SET PARADIGM
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·July 13, 2024
QUICK SET PARADIGM
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·July 13, 2024
ENDO ILS 29MM, CURVED
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 30, 2010
INSIGNIA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 11, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 2, 2014