Bausch + Lomb, Incorporated
Bausch + Lomb, Incorporated has 0 FDA recalls, 0 inspections, 6 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Nov 17, 2023
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 6 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 26, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K230954 | Samfilcon B Custom Contact Lens | Nov 17, 2023 |
| K211786 | Independent Corneal Viewing Chamber (IVC-21) | Dec 3, 2021 |
| K200528 | Bausch + Lomb (Kalifilcon A) Soft Contact Lens, Bausch + Lomb (Kalifilcon A) Soft Contact Lens for… | Jun 2, 2020 |
| K171404 | BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B) | Jul 17, 2017 |
| K170052 | Stellaris Elite vision enhancement system | Apr 19, 2017 |
| K162342 | Stellaris Elite Vision Enhancement System | Mar 24, 2017 |