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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