The following data is part of a premarket notification filed by Fine Advanced Compound Co., Ltd with the FDA for Non-sterile Zirconia Block.
| Device ID | K190112 |
| 510k Number | K190112 |
| Device Name: | Non-Sterile Zirconia Block |
| Classification | Powder, Porcelain |
| Applicant | Fine Advanced Compound Co., Ltd 7, Galgot-gil, Jinwi-myeon Pyeongtaek, KR |
| Contact | Jeong Kwang-ho |
| Correspondent | Chris Park Med.com 1809 Holland Dr Somerset, NJ 08873 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-01-23 |
| Decision Date | 2019-12-20 |