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 |