7 results
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18ms
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Sources: EU EUDAMED, US FDA
OLYMPUS IMAGEMANAGER SYSTEM VERSION 6.0 FOR WINDOWS
FDA 510(k)
FDA Class 1
·Radiology
NeoSculpt Plus
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
POROUS TITANIUM ACETABULAR AUGMENTS
FDA 510(k)
FDA Class 3
·Orthopedic
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 9, 2013
VITROS 5,1 FS CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·January 7, 2011
SETROX S 45
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVN·July 23, 2014
Sybaritic, NannoLight MP50. Model Numbers and Description: 1.) 304207-MP 220 Volt, Multi-Platform configuration (able to attach optional laser handpiece when purchased separately), Subassembly (unit only, no safety glasses, owner's manual, etc. included); 2.) 404207 Completed unit (safety glasses, owner's manual, etc. included), glossy finish, 220 Volt; 3.) 404207-MP Completed unit, matte finish, 220 Volt, Multi-Platform configuration; 4.) 404207-B Completed unit, matte finish, 220 Volt; 5.) 404207-USAB Completed unit, matte finish, 220 Volt, USA-style power cord; 6.) 404208-B Completed unit, matte finish, 110 Volt; and 7.) 404208-MP Completed unit, matte finish, 110 Volt, Multi-Platform configuration. The NannoLight Intense Pulsed Light System is indicated for use in surgical, aesthetic and cosmetic applications requiring selective photothermolysis (photocoagulation or coagulation) and hemostasis of soft tissue in the medical specialties of general and plastic surgery and dermatology.
FDA Recall
Terminated
·Sybaritic, Inc·Product code GEX·April 12, 2008