41 results
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31ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Flexylon Surgical Powder Free Gloves with Low Dermatitis Potential Claim, Green Tested For Use with 13 Chemotherapy Drugs; Flexylon Surgical Powder Free Gloves with Low Dermatitis Potential Claim, White Tested For Use with 32 Chemotherapy Drugs
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
FASTIN ORTHOCORD
FDA UDI
Medos International Sàrl·10886705008711·FASTIN RC w/ORTHOCORD Titanium Anchor with two ...
CYNOSURE, LLC
FDA registration
CYNOSURE, LLC·23 products·🇺🇸 United States
Buzzy® (models: Mini Healthcare, XL Healthcare, Mini Personal, XL Personal, Pro); VibraCool® (models: Easy Fit, Extended, Plantar, Flex, Pro DME, Pro UE, Pro LE, Pro 200H)
FDA 510(k)
FDA Class 1
·Physical Medicine
HOVEROUND REHAB SEATING SYSTEM FOR POWER WHEELCHAIRS
FDA 510(k)
FDA Class 2
·Physical Medicine
ICON LASER SYSTEM
FDA Adverse Event
Injury
·Product code GEX·March 27, 2014
ICON LASER SYSTEM
FDA Adverse Event
Injury
·Product code GEX·March 27, 2014
ELITE MD
FDA Adverse Event
Injury
·CYNOSURE, INC.·Product code GEX·January 7, 2014
ELITE MD
FDA Adverse Event
Malfunction
·CYNOSURE, INC.·Product code GEX·December 5, 2013
SMARTLIPO,600UM FIBER,SINGLE,STERILE
FDA Adverse Event
Malfunction
·CYNOSURE LLC·Product code GEX·January 14, 2022
VECTUS
FDA Adverse Event
Malfunction
·CYNOSURE LLC·Product code GEX·October 15, 2021
ELITE
FDA Adverse Event
Malfunction
·CYNOSURE, INC.·Product code GEX·December 5, 2013
ICON LASER SYSTEM
FDA Adverse Event
Injury
·Product code GEX·January 13, 2014
PICOSURE
FDA Adverse Event
Malfunction
·Product code GEX·November 12, 2021
ELITE MD
FDA Adverse Event
Malfunction
·CYNOSURE LLC·Product code GEX·June 28, 2024
ELITE MD
FDA Adverse Event
Malfunction
·CYNOSURE LLC·Product code GEX·June 28, 2024
CLARITY II
FDA Adverse Event
Malfunction
·LUTRONIC CORPORATION·Product code GEX·October 2, 2025
ICON LASER SYSTEM
FDA Adverse Event
Injury
·Product code GEX·January 13, 2014
ELITE+
FDA Adverse Event
Malfunction
·CYNOSURE LLC·Product code GEX·July 17, 2024
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
UNKNOWN·Product code ITJ·November 4, 2014