# Eiger Diagnostics, Inc. (manufacturer, Las Vegas, NV): 3 new FDA device listings, incl. device, general purpose, microbiology, diagnostic

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Eiger Diagnostics, Inc. |
| Role | Manufacturer |
| Establishment types | Manufacture Device in the United States for Export Only |
| Location | Las Vegas, NV, US |
| New listings | 3 |
| Devices | Device, General Purpose, Microbiology, Diagnostic; Enzyme Linked Immunosorbent Assay, T. Cruzi; Reagent, Leishmanii Serological |
| Product codes | LIB, MIU, LOO |
| Device classes | Class I |
| Medical specialties | Microbiology |
| Brand names | Echinococcus Microwell ELISA Kit; Leptospira Microwell ELISA Kit; Taenia Solium Microwell ELISA Kit; Opisthorchis Microwell ELISA Kit; Gnathostoma Microwell ELISA Kit; Spirometra Microwell ELISA Kit; Strongyloides Microwell ELISA Kit; Trichinella Microwell ELISA Kit |
| First new listing | 2026-06-01 |
| Latest new listing | 2026-06-01 |
| FDA registration number | 3026241718 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- 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.