The following data is part of a premarket notification filed by Dentalmax Co., Ltd. with the FDA for Luxen Cl Dental Liquid.
Device ID | K212548 |
510k Number | K212548 |
Device Name: | LUXEN CL Dental Liquid |
Classification | Powder, Porcelain |
Applicant | DENTALMAX Co., Ltd. 50-7, Pungsesandan 2-Ro, Pungse-Myeon, Dongnam-Gu Cheonan-si, KR 31217 |
Contact | Park Seung Bum |
Correspondent | Priscilla Chung LK Consulting Group USA, Inc. 18881 Von Karman Ave. STE 160 Irvine, CA 92612 |
Product Code | EIH |
CFR Regulation Number | 872.6660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-08-13 |
Decision Date | 2021-12-06 |
Summary: | summary |