The following data is part of a premarket notification filed by Megagen Implant Co., Ltd with the FDA for Mini Internal Implant System.
| Device ID | K150537 |
| 510k Number | K150537 |
| Device Name: | MiNi Internal Implant System |
| Classification | Implant, Endosseous, Root-form |
| Applicant | MEGAGEN IMPLANT CO., LTD 472, HANJANGGUN-RO, JAIN-MYEON Gyeongsan-si, KR 712-852 |
| Contact | Dong Guk Ha |
| Correspondent | Megan Hold KODENT, INC. 325 N. PUENTE ST., UNIT B Brea, CA 92821 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-03-03 |
| Decision Date | 2015-07-21 |
| Summary: | summary |