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FDA 510(k) Applications Submitted by ORMCO CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K061481
05/30/2006
GRENGLOO
ORMCO CORP.
K052477
09/09/2005
DAMON 3 MODIFIED
ORMCO CORP.
K062856
09/25/2006
TF ROTARY NICKEL TITANIUM FILE
ORMCO CORP.
K141611
06/16/2014
LYTHOS DIGITAL IMPRESSION SYSTEM
ORMCO CORP.
K955333
11/21/1995
SPIRIT MB
ORMCO CORP.
K081415
05/20/2008
DAMON 4CLEAR
ORMCO CORP.
K121524
05/23/2012
INSIGNIA
ORMCO CORP.
K101676
06/15/2010
CLEARARCH
ORMCO CORP.
K081900
07/03/2008
TEMPORARY TOOTH REPLACEMENT
ORMCO CORP.
K122065
07/13/2012
DIGITAL IMPRESSION SYSTEM FOR ORTHODONTIC USE
ORMCO CORP.
K112640
09/12/2011
HYPERELASTIC WIRE
ORMCO CORP.
K123118
10/03/2012
INSIGNIA DIGICAST
ORMCO CORP.
K123416
11/06/2012
INSIGNIA WITH ITERO
ORMCO CORP.
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