# Universal Brain Inc. (specification developer, Palo Alto, CA): 3 new FDA device listings, incl. stimulator, auditory, evoked response

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Universal Brain Inc. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Palo Alto, CA, US |
| New listings | 3 |
| Devices | Stimulator, Auditory, Evoked Response; Non-Normalizing Quantitative Electroencephalograph Software; Full-Montage Standard Electroencephalograph |
| Product codes | GWJ, OLT, GWQ |
| Device classes | Class II |
| Medical specialties | Neurology |
| Brand names | UB ERP System |
| First new listing | 2026-09-19 |
| Latest new listing | 2026-09-19 |
| FDA registration number | 3038896098 |
| 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.