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 |