Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Resin, Denture, Relining, Repairing, Rebasing
510(k) Number K063626
FOIA Releasable 510(k) K063626
Device Name DURAFLEX
Applicant
Cosmetic Dental Materials, Inc.
812 Water St. NE
Albany,  OR  97321
Applicant Contact ROBERT BOWERS
Correspondent
Cosmetic Dental Materials, Inc.
812 Water St. NE
Albany,  OR  97321
Correspondent Contact ROBERT BOWERS
Regulation Number872.3760
Classification Product Code
EBI  
Date Received12/06/2006
Decision Date 02/08/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-