K152175 is an FDA 510(k) clearance for the Upcera Dental Zirconia Blank for Aesthetic Restoration. This device is classified as a Powder, Porcelain (Class II - Special Controls, product code EIH).
Submitted by Liaoning Upcera Co., Ltd. (Benxi, CN). The FDA issued a Cleared decision on December 4, 2015, 122 days after receiving the submission on August 4, 2015.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6660.
| 510(k) Number | K152175 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 04, 2015 |
| Decision Date | December 04, 2015 |
| Days to Decision | 122 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EIH — Powder, Porcelain |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.6660 |