# Tz Medical, Inc. (repackager or relabeler, Tualatin, OR): 1 new FDA device listing, incl. electrosurgical patient return electrode

**Score:** 60/100

| Field | Value |
|---|---|
| Establishment | Tz Medical, Inc. |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Tualatin, OR, US |
| New listings | 1 |
| Devices | Electrosurgical Patient Return Electrode |
| Product codes | ODR |
| Device classes | Class II |
| Medical specialties | General, Plastic Surgery |
| Brand names | Ground Pad; P-411-V1 |
| First new listing | 2026-10-19 |
| Latest new listing | 2026-10-19 |
| FDA registration number | 3027815 |
| Registration expires | 2027-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- 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.