Class Class II

Essilor® Stellest® (DEN250016)

DEN250016 2025-09-25 Direct
Home/ Devices/ Essilor® Stellest® (DEN250016)

Description

Essilor® Stellest® by Essilor of America, Inc., an FDA 510(k) cleared ophthalmic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberDEN250016
Clearance Date2025-09-25
Clearance TypeDirect
Product CodeQUR
Regulation Number886.5845

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top