K223706 is an FDA 510(k) clearance for the PMMA BLOCK. This device is classified as a Crown And Bridge, Temporary, Resin (Class II - Special Controls, product code EBG).
Submitted by Huliang(Shanghai) Bio-Tech Co., Ltd. (Shanghai, CN). The FDA issued a Cleared decision on May 12, 2023, 151 days after receiving the submission on December 12, 2022.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3770.
| 510(k) Number | K223706 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 12, 2022 |
| Decision Date | May 12, 2023 |
| Days to Decision | 151 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EBG - Crown And Bridge, Temporary, Resin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3770 |