LFD
- Product code
- LFD
- Device name
- Saliva, Artificial
- Device class
- Class U
- Medical specialty
- Unknown
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 4
- Summaries archived here
- 1 (direct download)
- 510(k) clearances (all years, FDA)
- 50 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (4)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K253778 | 2026-02-27 | Elevate Oral Care | Allday Moisturizing Rinse | FDA |
| K250390 | 2025-05-19 | Rowpar Pharmaceuticals, Inc. | CloSYS® Dry Mouth Sensitive Mouth Rinse | FDA |
| K240508 | 2024-04-19 | Laclede, Inc. | Salivea Dry Mouth Moisturizing Gel (Dry Mouth Moistu | FDA |
| K234015 | 2024-03-11 | Eusa Pharma (Uk) Limited | Caphosol® Artifical Saliva (32 doses sachet box) |
Official FDA classification page: LFD
Classification and pathway per current FDA publications. Data from openFDA (CC0).