Company ยท US
Satelec - Acteon Group
FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2024. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 11, 2024 | K233922 | SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LO Satelec - Acteon Group, FR | ELC |
| May 3, 2018 | K172137 | PIEZOTOME CUBE Satelec - Acteon Group, FR | DZI |
| Apr 11, 2014 | K131906 | SCANWAVE PEN (WITH LIGHT GRAY CORD), SCANWAVE PEN (WITH MEDIUM GRAY CORD), SCANWAVE PEN (WITH DARK GRAY CORD), SCANWAVE Satelec - Acteon Group | EBZ |
| Mar 11, 2014 | K132322 | NEWTRON P5 XS B.LED Satelec - Acteon Group | ELC |
| Mar 10, 2014 | K132267 | NEWTRON P5, NEWTRON P5 B.LED Satelec - Acteon Group | ELC |
| Jan 16, 2014 | K131151 | ENDOCENTER Satelec - Acteon Group | ELC |
| Nov 26, 2013 | K131997 | NEWTRON BOOSTER Satelec - Acteon Group | ELC |
| Feb 23, 2012 | K113430 | PROULTRA PIEZO ULTRASONIC Satelec - Acteon Group | ELC |
| Jan 10, 2012 | K111623 | I-ENDO DUAL Satelec - Acteon Group | EBW |
| Nov 19, 2007 | K072030 | IMPLANT CENTER Satelec - Acteon Group | DZI |
| Aug 24, 2007 | K071424 | PMAX NEWTRON XS Satelec - Acteon Group | ELC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||