The following data is part of a premarket notification filed by Biogenesis Co., Ltd. with the FDA for Biogensis Implant System-kisses.
Device ID | K142813 |
510k Number | K142813 |
Device Name: | Biogensis Implant System-Kisses |
Classification | Implant, Endosseous, Root-form |
Applicant | BIOGENESIS CO., LTD. Mecha Zone #1109, SK Techno Park,50, Wanam-Ro, Seongsan Changwon-si, KR 642-971 |
Contact | Haeyong Lee |
Correspondent | Priscilla Chung LK Consulting Group USA, Inc. 2651 E Chapman Ave Ste 110 Fullerton, CA 92833 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-09-29 |
Decision Date | 2015-07-31 |
Summary: | summary |