# Ortho-Med, Inc. (repackager or relabeler, Tigard, OR): 6 new FDA device listings, incl. tray, surgical, instrument

**Score:** 50/100

| Field | Value |
|---|---|
| Establishment | Ortho-Med, Inc. |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Tigard, OR, US |
| New listings | 6 |
| Devices | Tray, Surgical, Instrument; Guide, Surgical, Instrument; Awl; Clamp, Surgical, General & Plastic Surgery; Stripper, Surgical; Tray, Surgical, Needle |
| Product codes | FSM, FZX, HWJ, GDJ, HRT, FSH |
| Device classes | Class I |
| Medical specialties | General, Plastic Surgery, Orthopedic |
| Brand names | Ortho-Med Inc |
| First new listing | 2026-06-16 |
| Latest new listing | 2026-07-14 |
| FDA registration number | 3019455 |
| Registration expires | 2027-12-31 |

## Why this score
- 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.