DeviceClearance

Product code LRX— Ophthalmic

CONTACT LENS CASE

Classification name
Case, Contact Lens
Device class
Class 2
Regulation
21 CFR 886.5928
Advisory panel
Ophthalmic
Total cleared
82
First cleared
Most recent

Market context for product code LRX

FDA has cleared 82 devices under product code LRX between 1984 and 2026, filed by 58 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code LRX

Recent clearances under product code LRX

Data sourced from openFDA. This site is unofficial and independent of the FDA.