K262074
- 510(k) number
- K262074
- Device name
- Any-Zircos
- Applicant
- Mediclus Co., Ltd. KR
- Product code
- EIH — Powder, Porcelain
- Decision date
- 2026-08-21
- Date received
- 2026-06-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K262074.pdf
Official FDA record: K262074
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.