K253845
- 510(k) number
- K253845
- Device name
- Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)
- Applicant
- Ram.Shaw Pte. , Ltd. SG
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2026-03-03
- Date received
- 2025-12-02
- 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: K253845.pdf
Official FDA record: K253845
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.