Medical Device Manufacturer · US , Mt. Laurel , NJ

Satelec - Acteon Group - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2007

Total

Cleared

Denied

Satelec - Acteon Group has 11 FDA 510(k) cleared dental devices. Based in Mt. Laurel, US.

Latest FDA clearance: Mar 2024. Active since 2007.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Satelec - Acteon Group

11 devices

1-11 of 11

SCANWAVE PEN (WITH LIGHT GRAY CORD), SCANWAVE PEN (WITH MEDIUM GRAY CORD),...

NEWTRON P5, NEWTRON P5 B.LED

PROULTRA PIEZO ULTRASONIC

Satelec - Acteon Group - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Satelec - Acteon Group

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