The following data is part of a premarket notification filed by Megagen Implant Co., Ltd. with the FDA for Anyridge Octa 1 Implant System.
| Device ID | K182448 |
| 510k Number | K182448 |
| Device Name: | AnyRidge Octa 1 Implant System |
| Classification | Implant, Endosseous, Root-form |
| Applicant | MegaGen Implant Co., Ltd. 45, Secheon-ro, 7-gil, Dasa-eup, Dalesong-gun Daegu, KR |
| Contact | Hyejin Jung |
| Correspondent | Priscilla Chung LK Consulting Group USA, Inc. 690 Roosevelt Irvine, CA 92620 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-09-07 |
| Decision Date | 2019-10-09 |
| Summary: | summary |