K262104
- 510(k) number
- K262104
- Device name
- Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)
- Applicant
- Ram.Shaw Pte., Ltd. SG
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2026-08-27
- Date received
- 2026-06-23
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K262104.pdf
Official FDA record: K262104
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.