FDA 510(k) Applications Submitted by Lars Moring

FDA 510(k) Number	Submission Date	Device Name	Applicant
K000163	01/19/2000	PM 2002 PROLINE/AEC	PLANMECA OY
K970263	01/23/1997	PM 2002 CC PROLINE	PLANMECA OY
K000428	02/09/2000	DIXI 2	PLANMECA OY
K060328	02/09/2006	PLANMECA PROMAX 3D	PLANMECA OY
K980581	02/17/1998	PLANMECA DIXI, DIGITAL INTRAORAL X-RAY IMAGING SYSTEM	PLANMECA OY
K160506	02/24/2016	Planmeca ProMax 3D Max, Planmeca Maximity	PLANMECA OY
K970812	03/05/1997	PM 2002 CC PROLINE	PLANMECA OY
K200572	03/05/2020	Planmeca Romexis	Planmeca Oy
K970975	03/17/1997	PROSTYLE INTRA	PLANMECA OY
K140713	03/21/2014	PLANMECA ROMEXIS	PLANMECA OY
K180918	04/09/2018	Planmed Verity	Planmed Oy
K961420	04/12/1996	PROSTYLE COMPACT	PLANMECA OY
K121418	05/11/2012	PLANMED VERITY	PLANMED OY
K171385	05/11/2017	Planmeca Romexis	Planmeca Oy
K962105	05/31/1996	PLANNED SOPHIED CLASSIC	PLANMED OY
K972033	06/02/1997	PLANMECA INTRACAM	PLANMECA OY
K181576	06/15/2018	Planmeca Viso	Planmeca Oy
K121963	07/05/2012	PLANMED NUANCE DIGIGUIDE	PLANMED OY
K072244	08/13/2007	PLANMECA PROONE	PLANMECA OY
K963209	08/16/1996	PROSTYLE COMPACT	PLANMECA OY
K192317	08/26/2019	Planmed Clarity 2D and Clarity S	Planmed Oy
K983659	10/19/1998	PLANMED SOPHIE & PLANNED SOPHIE CLASSIC	PLANMED OY
K984013	11/11/1998	PLANMECA INTRACAM STATION	PLANMECA OY
K093590	11/19/2009	PLANMECA PROMAX 3D MAX	PLANMECA OY
K163328	11/28/2016	Planmed Clarity	Planmed Oy
K143435	12/01/2014	Planmed Verity	PLANMED OY
K103689	12/17/2010	PLANMECA PROMAX 3D MID	PLANMECA OY