Essilor® Stellest®— 510(k) DEN250016
UnknownEssilor Of America, Inc.
FDA 510(k) clearance DEN250016 for Essilor® Stellest®, Unknown on 2025-09-25. Applicant: Essilor Of America, Inc.. Device class: 2.
Clearance details
- Applicant
- Essilor Of America, Inc.
- Product code
- Code QUR
- Device class
- Class 2
- Regulation
- 21 CFR 886.5845
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Dallas, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.