FDA 510(k) Applications for Medical Device Product Code "PME"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K163171 | Bisco, Inc. | CeraClean | 04/14/2017 |
| K152322 | DENALI CORPORATION | Resolve 2.0 | 12/16/2015 |
| K191133 | Kuraray Noritake Dental Inc. | KATANA Cleaner, KATANA Cleaner (Trial) | 10/08/2019 |
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