Planmeca Oy - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Planmeca Oy has 28 FDA 510(k) cleared radiology devices. Based in Helsinki, FI.
Last cleared in 2023. Active since 1993.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Planmeca Oy
28 devices
Cleared
Dec 28, 2023
Planmeca Viso
Radiology
266d
Cleared
Dec 02, 2020
Planmeca Romexis
Radiology
272d
Cleared
Sep 13, 2018
Planmeca Viso
Radiology
90d
Cleared
Nov 14, 2017
Planmeca Romexis
Radiology
187d
Cleared
May 20, 2016
Planmeca ProMax 3D Max, Planmeca Maximity
Radiology
86d
Cleared
Jun 16, 2014
PLANMECA ROMEXIS
Radiology
87d
Cleared
Mar 17, 2011
PLANMECA PROMAX 3D MID
Radiology
90d
Cleared
May 12, 2010
PLANMECA PROMAX 3D MAX
Radiology
174d
Cleared
Jul 29, 2009
PLANMECA PROSENSOR
Radiology
97d
Cleared
Sep 21, 2007
PLANMECA PROONE
Radiology
39d
Cleared
Mar 15, 2006
PLANMECA PROMAX 3D
Radiology
34d
Cleared
Jun 24, 2005
PLANMECA PROMAX WITH DEC (DYNAMIC EXPOSURE CONTROL)
Radiology
21d