K233356
- 510(k) number
- K233356
- Device name
- Illusion Aligner Pro: Illusion Aligner FLX
- Applicant
- Laxmi Dental Export Pvt., Ltd. IN
- Product code
- NXC — Aligner, Sequential
- Decision date
- 2024-08-08
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K233356.pdf
Official FDA record: K233356
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.