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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
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