K230947
- 510(k) number
- K230947
- Device name
- C.A.R.E. Appliance (DNA, mRNA, mmRNA)
- Applicant
- Vivos Therapeutics, Inc. KY · US
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2023-11-28
- Date received
- 2023-04-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K230947.pdf
Official FDA record: K230947
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.