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

FDA-registered makers of Lenses, Soft Contact, Daily Wear in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Lenses, Soft Contact, Daily Wear (product code LPL). 21 have a 510(k) clearance or PMA approval on file and 8 have a recall event. FDA data exported November 3, 2026.

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Device
Lenses, Soft Contact, Daily Wear
Product code
LPL
Country
United States

Makers of Lenses, Soft Contact, Daily Wear in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
X-Cel Specialty ContactsDuluth, GA, United StatesContract manufacturer, Contract sterilizer, Manufacturer17August 14, 2024100api.fda.gov
Alcon Research, LLCDuluth, GA, United StatesManufacturer, Repackager or relabeler, Specification developer17November 16, 2023070api.fda.gov
Alcon Research, LLCFort Worth, TX, United StatesSpecification developer17November 16, 2023020api.fda.gov
ABB Optical Group LLC.Kansas City, MO, United StatesManufacturer9December 10, 2002100api.fda.gov
Bausch & Lomb IncorporatedLancaster, NY, United StatesManufacturer10November 17, 2023010api.fda.gov
Bausch & Lomb IncorporatedRochester, NY, United StatesComplaint file establishment, Manufacturer, Specification developer10November 17, 2023020api.fda.gov
Johnson & Johnson Vision Care, Inc.Jacksonville, FL, United StatesComplaint file establishment, Manufacturer10November 29, 2021070api.fda.gov
Metro Optics of Austin, Inc.Pflugerville, TX, United StatesManufacturer9February 6, 2024100api.fda.gov
COOPERVISION Manufacturing Puerto Rico, LLCJuana Diaz, PR, United StatesComplaint file establishment, Manufacturer9February 4, 2022020api.fda.gov
Bausch & Lomb IncorporatedClearwater, FL, United StatesManufacturer7October 30, 2014100api.fda.gov
Benz Research And Development LLCSarasota, FL, United StatesContract manufacturer, Contract sterilizer, Manufacturer7August 9, 2010000api.fda.gov
Bausch & Lomb IncorporatedLynchburg, VA, United StatesManufacturer7June 2, 2020000api.fda.gov
Art Optical Contact Lens, Inc.Walker, MI, United StatesManufacturer3September 14, 2010000api.fda.gov
Coopervision, Inc.Scottsville, NY, United StatesComplaint file establishment, Manufacturer3May 30, 2013020api.fda.gov
Visioneering Technologies, IncAlpharetta, GA, United StatesManufacturer3November 7, 2017000api.fda.gov
Advanced Vision TechnologiesLakewood, CO, United StatesManufacturer2August 23, 2012000api.fda.gov
AcuconSarasota, FL, United StatesManufacturer2July 18, 2005020api.fda.gov
TANGIBLE SCIENCE IncCampbell, CA, United StatesSpecification developer2December 13, 2017000api.fda.gov
United Contact Lens IncArlington, WA, United StatesManufacturer2July 1, 2005000api.fda.gov
Acuity Polymers Inc.Rochester, NY, United StatesComplaint file establishment, Specification developer1May 13, 2013000api.fda.gov
Meti Optical IncDover, DE, United StatesSpecification developer1March 20, 2025000api.fda.gov
Kontur Kontact Lens Co., Inc.Hercules, CA, United StatesManufacturer0000api.fda.gov
Orion VisionMarietta, GA, United StatesContract manufacturer0000api.fda.gov

Updated November 3, 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.