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 |