Data / Medical devices / United States / Visionary Contact Lens, Inc.
Visionary Contact Lens, Inc.: FDA-registered device maker in Anaheim, CA, United States, 1 PMA approval
Visionary Contact Lens, Inc. is registered with the FDA (registration 3002830597) in Anaheim, CA, United States. It lists 3 device types. The FDA files 1 PMA approval under its listings, the newest dated February 10, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3002830597
- Address
- 2940 East Miraloma Ave., Anaheim, CA, United States, 92806
- Owner or operator
- VISIONARY CONTACT LENS, Inc. (9031595)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- September 6, 2006
- Registered through
- 2026
- Brand names listed
- GOV Overnight Ortho-K Lens, Optimum GP, Optimum Extra, and GOV Lens, Optimum Infinite, Hyper GP, and GOV Lens, RG5 Overnight Ortho-K Lens, Visionary
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lens, Contact (Orthokeratology) | MUW | 2 | Contract manufacturer | accessdata.fda.gov |
| Lens, Contact (Other Material) - Daily | HQD | 2 | Contract manufacturer | accessdata.fda.gov |
| Lens, Contact, Orthokeratology, Overnight | NUU | 3 | Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| February 10, 2026 | P240045 | Optimum Infinite (tisilfocon A) Orthokeratology Lenses II | NUU | 0 | February 10, 2026 | accessdata.fda.gov |
Compare with other makers
- All makers of Lens, Contact (Orthokeratology)
- All makers of Lens, Contact (Other Material) - Daily
- All makers of Lens, Contact, Orthokeratology, Overnight
Updated February 10, 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.