8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEONICS ALUMINA C-TAPER HEAD, OSTEONICS TRIDENT POLYETHYLENE INSERTS
FDA 510(k)
FDA Class 2
·Orthopedic
DEXIDE DISPOSABLE SURGICAL SCRUB BRUSH
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ACTA VESSEL OCCLUSION SYSTEM (VOS)
FDA 510(k)
FDA Class 2
·Cardiovascular
INVISION-PLUS
FDA Adverse Event
Malfunction
·RYMED TECHNOLOGIES, LLC·Product code FPA·July 7, 2022
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·March 14, 2025
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 7, 2013
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014
CAPSURE EPI
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DTB·February 15, 2011