• 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 Abutment, Implant, Dental, Endosseous
510(k) Number K232560
Device Name Angled Abutment
Applicant
Arum Dentistry Co., Ltd.
23, Gukjegwahak 11-ro, Yuseong-gu
Daejeon,  KR 34002
Applicant Contact Won-yi Choi
Correspondent
Arum Dentistry Co., Ltd.
23, Gukjegwahak 11-ro, Yuseong-gu
Daejeon,  KR 34002
Correspondent Contact Won-yi Choi
Regulation Number872.3630
Classification Product Code
NHA  
Date Received08/23/2023
Decision Date 12/19/2023
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-