7 results
·
35ms
·
Sources: EU EUDAMED, US FDA
APLICARE ONE ACETONE ALCOHOL SWABSTICK
FDA 510(k)
FDA Unclassified
·Unknown
RECLEAR PHOTOTHERAPY SYSTEM, MODEL FGCM0012
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Surgical Gown (40083)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
S-ROM M HEAD 36MM -3
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 27, 2014
UNKNOWN M2A CUP
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·November 15, 2012
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·September 9, 2010
Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228. (Azurion 3 M12, Azurion 3 M15, Azurion 5 M12, Azurion 5 M20, Azurion 7 B12, Azurion 7 B20, Azurion 7 M12, Azurion 7 M20)
FDA Enforcement
Class II
·Terminated·Philips North America Llc·November 17, 2021