7 results
·
25ms
·
Sources: EU EUDAMED, US FDA
LANCE LTD. STERI. STITCH CUTTER BLADE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
The Orthodontic Store
FDA UDI
Young Innovations, Inc.·00843471182819·.022 U/R Std. Weld Size #17
INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE
FDA 510(k)
FDA Class 2
·Neurology
SUCTION INSTRUMENT, MACBICK DIS. FRAZ.
FDA 510(k)
FDA Class 2
·General Hospital
MACROLYTE DISPERSIVE ELECTRODE, PREMIE SINGLE DISPERSIVE WITH 10 FOOT CABLE
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code GEI·April 24, 2014
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code LYJ·October 3, 2012
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 21, 2010