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Candela Laser Corporation

8 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Candela Corporation Vbeam Aesthetica Laser System, Model/Catalog # 9914-00-0320 Vbeam Aest recall (Z-0508-2007)Candela Laser Corporation2007-02-15
Candela Corporation Vbeam Aesthetica Laser System, Model/Catalog # 9914-08-0320 Vbeam Aest recall (Z-0509-2007)Candela Laser Corporation2007-02-15
Candela Corporation Vbeam Platinum Laser System, Model/Catalog # 9914-00-0310 Vbeam Platin recall (Z-0510-2007)Candela Laser Corporation2007-02-15
Candela Corporation Vbeam Platinum Laser System, Model/Catalog # 9914-08-0310 Vbeam Platin recall (Z-0511-2007)Candela Laser Corporation2007-02-15
Candela Corporation Vbeam Perfecta Laser System, Model/Catalog # 9914-00-0300 Vbeam Perfec recall (Z-0512-2007)Candela Laser Corporation2007-02-15
Candela Corporation Vbeam Perfecta Laser System, Model/Catalog # 9914-08-0300 Vbeam Perfec recall (Z-0513-2007)Candela Laser Corporation2007-02-15
Candela Laser VBeam Perfecta, a Pulsed Dye Laser used for General Surgery, Dermatology, Gy recall (Z-0842-06)Candela Laser Corporation2006-05-04
Candela Smoothbeam Laser System Model Numbers: 9914-00-0820 9914-06-0820 9914-07-0820 9914 recall (Z-0291-04)Candela Laser Corporation2004-01-01

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Every clearance here is in the API, with alerts when new ones post.