The following data is part of a premarket notification filed by Dentium Co., Ltd. with the FDA for Nr Line Implant System.
Device ID | K153268 |
510k Number | K153268 |
Device Name: | NR Line Implant System |
Classification | Implant, Endosseous, Root-form |
Applicant | DENTIUM CO., LTD. 29 TEHERAN-RO, 87-GZL GANGNAM-GU Seoul, KP 06167 |
Contact | Younjung Yuk |
Correspondent | Claude Berthoin DENTERPRISE INTERNATIONAL, INC. 100 EAST GRANADA BLVD SUITE 219 Ormond Beach, FL 32176 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-11-12 |
Decision Date | 2016-07-20 |