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12 devices found
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Manufacturer: Satelec - Acteon Group
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Device · Manufacturer · Authorizations
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Status
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Registry
Class
Scanwave Pen (With Light Gray Cord), Scanwave Pen (With Medium Gray Cord), Scanwave Pen (With Dark Gray Cord), Scanwave
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K131906
Active
Cleared 11 Apr 2014
Active
510(k)
510(k)
II
I-Endo Dual
Satelec - Acteon Group
·
,
FDA registration: France
Class I
FDA 510(k)
K111623
Active
Cleared 10 Jan 2012
Active
510(k)
510(k)
I
Newtron Booster
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K131997
Active
Cleared 26 Nov 2013
Active
510(k)
510(k)
II
Implant Center
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K072030
Active
Cleared 19 Nov 2007
Active
510(k)
510(k)
II
Proultra Piezo Ultrasonic
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K113430
Active
Cleared 23 Feb 2012
Active
510(k)
510(k)
II
Newtron P5 Xs B.led
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K132322
Active
Cleared 11 Mar 2014
Active
510(k)
510(k)
II
PIEZOTOME M+, PIEZOTOME M+ Handpiece
Satalec-Acteon Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K163610
Active
Cleared 19 May 2017
Active
510(k)
510(k)
II
Pmax Newtron Xs
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K071424
Active
Cleared 24 Aug 2007
Active
510(k)
510(k)
II
Endocenter
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K131151
Active
Cleared 16 Jan 2014
Active
510(k)
510(k)
II
Sp Newtron Can-A; Module Newtron Can-A Emb; Support Xinetic; Nwt Can Slim Led Cord G3 Short; Nwt Can Slim Led Cord G3 Long
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K233922
Active
Cleared 11 Mar 2024
Active
510(k)
510(k)
II
Piezotome Cube
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K172137
Active
Cleared 3 May 2018
Active
510(k)
510(k)
II
Newtron P5, Newtron P5 B.led
Satelec - Acteon Group
·
,
FDA registration: France
Class II
FDA 510(k)
K132267
Active
Cleared 10 Mar 2014
Active
510(k)
510(k)
II
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