Clearance Summary
Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank received FDA 510(k) clearance under submission number K212259, sponsored by Zirdent New Material Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-11-12.
- Submission: K212259
- Applicant / Sponsor: Zirdent New Material Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6660
- Decision date: 2021-11-12
Classification & Regulation
This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.