# Ray Vision Inc. (specification developer, Lake Forest, CA): 18 new FDA device listings, incl. retinoscope, ac-powered

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Ray Vision Inc. |
| Owner / operator | Ray Vision Inc |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Lake Forest, CA, US |
| New listings | 18 |
| Devices | Retinoscope, Ac-Powered; Ophthalmoscope, Ac-Powered; Perimeter, Automatic, Ac-Powered; System, Imaging, Pulsed Echo, Ultrasonic; Transducer, Ultrasonic, Diagnostic; Prism, Bar, Ophthalmic; Simulatan (Including Crossed Cylinder); Clip, Lens, Trial, Ophthalmic; Perimeter, Manual; Exophthalmometer |
| Product codes | HKL, HLI, HPT, IYO, ITX, HKW, HOR, HPB, HON, HLS, MMF, MSG, HOO, HLJ |
| Device classes | Class I, Class II |
| Medical specialties | Ophthalmic, Radiology |
| Brand names | Ray Vision Retinoscope; Ray Vision Ophthalmoscope, ac-powered; Ray Vision Perimeter; Ray Vision Ultrasound Biomicroscope; Ray Vision Prism Bar; Ray Vision Cross Cylinder; Ray Vision Trial Lens Clip Set; Ray Vision Ultrasonic A/B Scanner for Ophthalmology |
| First new listing | 2026-05-26 |
| Latest new listing | 2026-05-27 |
| FDA registration number | 3013436538 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.