Data / Medical devices / Lenses, Soft Contact, Daily Wear

Lenses, Soft Contact, Daily Wear (LPL): 69 FDA-registered makers in 18 countries

69 establishments in 18 countries are registered with the FDA to make Lenses, Soft Contact, Daily Wear (product code LPL, Class 2, 21 CFR 886.5925). 67 of them have a 510(k) clearance or PMA approval on file and 8 have a recall event. The FDA has issued 489 510(k) clearances under this code, the latest on October 23, 2026, and lists 40 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

LPL

Device class

2

Regulation

886.5925

Medical specialty

Ophthalmic

Makers by country

Makers of Lenses, Soft Contact, Daily Wear

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Updated October 23, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.