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 |