The following data is part of a premarket notification filed by Dentium Co., Ltd. with the FDA for Dentium Implantium & Superline Prosthetics.
| Device ID | K160828 |
| 510k Number | K160828 |
| Device Name: | Dentium Implantium & SuperLine Prosthetics |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | DENTIUM CO., LTD. 150, EONDONG-RO, GIHEUNG-GU Yongin-si, KR 443-270 |
| Contact | Sangpil Yoon |
| Correspondent | Sangpil Yoon DENTIUM CO., LTD. 150, EONDONG-RO, GIHEUNG-GU Yongin-si, KR 443-270 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-03-25 |
| Decision Date | 2016-09-15 |
| Summary: | summary |