The following data is part of a premarket notification filed by Dentsply Sirona with the FDA for Mis Angulated Multi-unit Abutments.
| Device ID | K213432 |
| 510k Number | K213432 |
| Device Name: | MIS Angulated Multi-unit Abutments |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | Dentsply Sirona 221 West Philadelphia Street, Suite 60W York, PA 17401 |
| Contact | Courtney Clark |
| Correspondent | Courtney Clark Dentsply Sirona 221 West Philadelphia Street, Suite 60W York, PA 17401 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-10-22 |
| Decision Date | 2022-04-01 |