• 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, Root Canal Filling
510(k) Number K180199
Device Name BIO-C TEMP
Applicant
Angelus Industria de Produtos Odontologicos S/A
Rua Waldir Landgraf, 101
Londrina,  BR 86031-218
Applicant Contact Paulo Sergio Calixto de Oliveira
Correspondent
Angelus Industria de Produtos Odontologicos S/A
Rua Waldir Landgraf, 101
Londrina,  BR 86031-218
Correspondent Contact Juliana Norder
Regulation Number872.3820
Classification Product Code
KIF  
Date Received01/24/2018
Decision Date 01/04/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-