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Data / Medical devices / Lens, Contact (Other Material) - Daily / United States

FDA-registered makers of Lens, Contact (Other Material) - Daily in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Lens, Contact (Other Material) - Daily (product code HQD). 11 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

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Device
Lens, Contact (Other Material) - Daily
Product code
HQD
Country
United States

Makers of Lens, Contact (Other Material) - Daily in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Acuity Polymers Inc.Rochester, NY, United StatesComplaint file establishment, Specification developer14April 3, 2024100api.fda.gov
Bausch & Lomb IncorporatedWilmington, MA, United StatesManufacturer, Specification developer15February 12, 2019000api.fda.gov
Bausch & Lomb IncorporatedRochester, NY, United StatesComplaint file establishment, Manufacturer, Specification developer15February 12, 2019010api.fda.gov
Advanced Vision TechnologiesLakewood, CO, United StatesManufacturer4March 17, 2022000api.fda.gov
Paragon Vision Sciences, Inc.Gilbert, AZ, United StatesComplaint file establishment, Manufacturer2May 5, 2023000api.fda.gov
Synergeyes, Inc.Carlsbad, CA, United StatesComplaint file establishment, Manufacturer2November 15, 2016000api.fda.gov
Acculens, Inc.Golden, CO, United StatesContract manufacturer, Manufacturer1June 16, 2023000api.fda.gov
BostonSight/BostonSight Specialty Lenses/BostonSight TECHNeedham Hgts, MA, United StatesManufacturer1August 14, 2024010api.fda.gov
Contex, IncorporatedSherman Oaks, CA, United StatesManufacturer1August 28, 2000000api.fda.gov
Euclid Vision CorporationSterling, VA, United StatesManufacturer1April 3, 2002000api.fda.gov
Valley Contax, IncEugene, OR, United StatesContract manufacturer, Manufacturer1January 7, 2022000api.fda.gov
Art Optical Contact Lens, Inc.Walker, MI, United StatesContract manufacturer0000api.fda.gov
Aurora GP Lab IncGoodyear, AZ, United StatesContract manufacturer0000api.fda.gov
Bausch & Lomb IncorporatedLynchburg, VA, United StatesManufacturer0000api.fda.gov
Cler Vision Inc.Riverside, CA, United StatesContract manufacturer0000api.fda.gov
Hedgefog Research Inc.San Pedro, CA, United StatesContract manufacturer0000api.fda.gov
Visionary Contact Lens, Inc.Anaheim, CA, United StatesContract manufacturer0000api.fda.gov
Visionary Optics, LLCFront Royal, VA, United StatesContract manufacturer0000api.fda.gov
Visionary Optics, LLCSterling, VA, United StatesContract manufacturer0000api.fda.gov
X-Cel Specialty ContactsDuluth, 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.