DeviceClearance

Product code LPL— Ophthalmic

Pegavision (Toufilcon B) Daily Disposable Soft (Hydrophilic) Contact Lenses +1 more

Classification name
Lenses, Soft Contact, Daily Wear
Device class
Class 2
Regulation
21 CFR 886.5925
Advisory panel
Ophthalmic
Total cleared
486
First cleared
Most recent

Market context for product code LPL

FDA has cleared 486 devices under product code LPL between 1994 and 2026, filed by 142 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 LPL

Adverse events under product code LPL

product code LPL
Injury
988
Other
4
Total
992

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code LPL

1–100 of 486

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