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Satelec - Acteon Group

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K233922SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CANMarch 11, 2024
K172137PIEZOTOME CUBEMay 3, 2018
K131906SCANWAVE PEN (WITH LIGHT GRAY CORD), SCANWAVE PEN (WITH MEDIUM GRAY CORD), SCANWAVE PEN (WITH DARK GApril 11, 2014
K132322NEWTRON P5 XS B.LEDMarch 11, 2014
K132267NEWTRON P5, NEWTRON P5 B.LEDMarch 10, 2014
K131151ENDOCENTERJanuary 16, 2014
K131997NEWTRON BOOSTERNovember 26, 2013
K113430PROULTRA PIEZO ULTRASONICFebruary 23, 2012
K111623I-ENDO DUALJanuary 10, 2012
K072030IMPLANT CENTERNovember 19, 2007
K071424PMAX NEWTRON XSAugust 24, 2007