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 |