The following data is part of a premarket notification filed by Dentis Co. Ltd. with the FDA for Oneq-sl Implant System.
| Device ID | K142313 |
| 510k Number | K142313 |
| Device Name: | OneQ-SL Implant System |
| Classification | Implant, Endosseous, Root-form |
| Applicant | DENTIS CO. LTD. #951, WORAM-DONG, DALSEO-GU Daegu, KR 704-320 |
| Contact | Jeong Seop Keun |
| Correspondent | April Lee WITHUS GROUP INC 2531 PEPPERDALE DRIVE Rowland Heights, CA 91748 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-08-19 |
| Decision Date | 2015-12-10 |
| Summary: | summary |