# Gurin Products LLC (repackager or relabeler, Tustin, CA): 3 new FDA device listings, incl. electrode, cutaneous

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Gurin Products LLC |
| Owner / operator | Gurin Products, LLC |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Tustin, CA, US |
| New listings | 3 |
| Devices | Electrode, Cutaneous; Stimulator, Nerve, Transcutaneous, Over-The-Counter; Stimulator, Muscle, Powered, For Muscle Conditioning |
| Product codes | GXY, NUH, NGX |
| Device classes | Class II |
| Medical specialties | Neurology, Physical Medicine |
| Brand names | Adhesive Electodes; MEDVICE; Medvice Electro Therapy Massager MV950; Electro Therapy Massager MV950; Medvice ElectroTherapy Massager MV950 |
| First new listing | 2026-09-10 |
| Latest new listing | 2026-10-22 |
| FDA registration number | 3006793151 |
| Registration expires | 2027-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
- Listed in the last 45 days.

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: 2026-11-04T21:52:36.524Z.
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.