K233544
- 510(k) number
- K233544
- Device name
- MESHEET
- Applicant
- Dentis Co., Ltd. KR
- Product code
- NXC — Aligner, Sequential
- Decision date
- 2024-02-22
- Date received
- 2023-11-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K233544.pdf
Official FDA record: K233544
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.