Satelec - Acteon Group
Satelec - Acteon Group holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2024.
Top product codes for Satelec - Acteon Group
Recent clearances by Satelec - Acteon Group
- K233922 — SP NEWTRON CAN-A +4 more
- K172137 — PIEZOTOME CUBE
- K131906 — SCANWAVE PEN (WITH LIGHT GRAY CORD), SCANWAVE PEN (WITH MEDIUM GRAY CORD), SCANWAVE PEN (WITH DARK GRAY CORD), SCANWAVE
- K132322 — NEWTRON P5 XS B.LED
- K132267 — NEWTRON P5, NEWTRON P5 B.LED
- K131151 — ENDOCENTER
- K131997 — NEWTRON BOOSTER
- K113430 — PROULTRA PIEZO ULTRASONIC
- K111623 — I-ENDO DUAL
- K072030 — IMPLANT CENTER
- K071424 — PMAX NEWTRON XS
Data sourced from openFDA. This site is unofficial and independent of the FDA.