The following data is part of a premarket notification filed by Achimhai Medical Corporation with the FDA for Kisses Plus Implant System.
| Device ID | K172630 |
| 510k Number | K172630 |
| Device Name: | Kisses Plus Implant System |
| Classification | Implant, Endosseous, Root-form |
| Applicant | ACHIMHAI Medical Corporation 28, Namyang-ro, 930beon-gil, Namyang-eup Hwaseong-si, KR 18255 |
| Contact | Ji Ho 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 | 2017-09-01 |
| Decision Date | 2018-04-03 |
| Summary: | summary |