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 Material, Tooth Shade, Resin
510(k) Number K222445
Device Name LC ChromeFlow
Applicant
S&C Polymer Silicon- Und Composite Spezialitaten GmbH
Robert-Bosch-Str. 2
Elmshorn,  DE 25335
Applicant Contact Christian Boettcher
Correspondent
S&C Polymer Silicon- Und Composite Spezialitaten GmbH
Robert-Bosch-Str. 2
Elmshorn,  DE 25335
Correspondent Contact Christian Boettcher
Regulation Number872.3690
Classification Product Code
EBF  
Subsequent Product Code
EBC  
Date Received08/15/2022
Decision Date 03/06/2023
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
-
-