The following data is part of a premarket notification filed by Megagen Implant Co., Ltd. with the FDA for Anyone Onestage Implant System.
| Device ID | K210161 |
| 510k Number | K210161 |
| Device Name: | AnyOne Onestage Implant System |
| Classification | Implant, Endosseous, Root-form |
| Applicant | MegaGen Implant Co., Ltd. 45, Secheon-ro, 7-gil Daegu, KR 42921 |
| Contact | You Jung Kim |
| Correspondent | You Jung Kim DaeGyeong Regulatory Affairs Institute 32, Innovalley-ro Daegu, KR 41065 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-01-21 |
| Decision Date | 2021-06-22 |
| Summary: | summary |