26 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CONTOUR DESIGN GOLD EYELID IMPLANT, MODEL CONTOUR DESIGN (SERIES 3000)
FDA 510(k)
FDA Class 2
·Ophthalmic
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040011744·Zirlux 16+ White 95X14
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033336793·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033336779·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033336748·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033336755·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361011040·PedFuse RespondX, CNL, 5.0mm x 40mm
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033336762·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033336731·
KSEA MONOPOLAR VAPORIZATION ELECTRODES
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
FG-36UX, FIBER ULTRASOUND GASTROSCOPE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 30, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·October 4, 2013
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·October 4, 2013
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·October 4, 2013
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·October 4, 2013
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·October 2, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013