Satelec - Acteon Group
Satelec - Acteon Group appears in FDA public data with 0 recalls, 11 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Mar 11, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K233922 | SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN | Mar 11, 2024 |
| K172137 | PIEZOTOME CUBE | May 3, 2018 |
| K131906 | SCANWAVE PEN (WITH LIGHT GRAY CORD), SCANWAVE PEN (WITH MEDIUM GRAY CORD), SCANWAVE PEN (WITH DARK G | Apr 11, 2014 |
| K132322 | NEWTRON P5 XS B.LED | Mar 11, 2014 |
| K132267 | NEWTRON P5, NEWTRON P5 B.LED | Mar 10, 2014 |
| K131151 | ENDOCENTER | Jan 16, 2014 |
| K131997 | NEWTRON BOOSTER | Nov 26, 2013 |
| K113430 | PROULTRA PIEZO ULTRASONIC | Feb 23, 2012 |
| K111623 | I-ENDO DUAL | Jan 10, 2012 |
| K072030 | IMPLANT CENTER | Nov 19, 2007 |
| K071424 | PMAX NEWTRON XS | Aug 24, 2007 |