# Medinova Group Co. (manufacturer, Laguna Beach, CA): 21 new FDA device listings, incl. shield, eye, ophthalmic (including sunlamp protective eyewear and post

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Medinova Group Co. |
| Role | Manufacturer |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Manufacture Device in the United States for Export Only |
| Location | Laguna Beach, CA, US |
| New listings | 21 |
| Devices | Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear); Pad, Eye; Tape And Bandage, Adhesive; Applicator, Absorbent Tipped, Sterile; Disinfectant, Medical Devices; Container, Specimen Mailer And Storage, Non-Sterile; Dish, Tissue Culture; Punch, Gelfoam, Non-Sterile; Tray, Surgical, Instrument; Adhesive Backed Thermal Skin Patches |
| Product codes | HOY, HMP, KGX, KXG, LRJ, NNK, KIZ, NNT, FSM, OMW, IMD, HTD, OEA, KEW, DJG |
| Device classes | Class I, Class II |
| Medical specialties | Ophthalmic, General, Plastic Surgery, General Hospital, Pathology, Hematology, Ear, Nose, Throat, Physical Medicine, Clinical Toxicology, Microbiology |
| First new listing | 2026-05-09 |
| Latest new listing | 2026-05-09 |
| FDA registration number | 3044466317 |
| 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.