Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3026241718

FEI Number

3026241718

Entity Name

EIGER DIAGNOSTICS, INC.

City/State/Country

Las Vegas, NV, US

Establishment Address

6850 Paradise Rd, Las Vegas, NV 89119, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Eiger Diagnostics, Inc. (Owner Number: 10087288)

Owner / Operator Contact Address

6850 Paradise Road, Las Vegas, NV 89119, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

E. histolytica Microwell ELISA Kit Fasciola gigantica Microwell ELISA Kit Taenia Solium Microwell ELISA Kit Opisthorchis Microwell ELISA Kit Schistosoma Microwell ELISA Kit Angiostrongylus Microwell ELISA Kit Paragonimus Microwell ELISA Kit Gnathostoma Microwell ELISA Kit Ancylostoma Microwell ELISA Kit Leptospira Microwell ELISA Kit Spirometra Microwell ELISA Kit Toxocara Microwell ELISA Kit Fasciola hepatica Microwell ELISA Kit Strongyloides Microwell ELISA Kit Ascaris Microwell ELISA Kit Clonorchis Microwell ELISA Kit Echinococcus Microwell ELISA Kit Filariasis Microwell ELISA Kit Trichinella Microwell ELISA Kit Eiger Diagnostics Clonorchis ELISA Eiger Diagnostics Paragonimus ELISA Schistosoma IgG, Schistosoma IgM Eiger Diagnostics Schistosoma ELISA Eiger Diagnostics Echinococcus ELISA Eiger Diagnostics Leishmania ELISA Eiger Diagnostics Chagas ELISA T. solium (IgG/IgM) Eiger Diagnostics Angiostrongylus ELISA Eiger Diagnostics Filariasis ELISA Eiger Diagnostics Toxocara ELISA Trichinella IgG , Trichinella IgM Eiger Diagnostics Gnathostoma ELISA Eiger Diagnostics Trichinella ELISA Eiger Diagnostics Strongyloides ELISA Eiger Diagnostics Fasciola ELISA Eiger Diagnostics Ascaris ELISA Eiger Diagnostics Ancylostoma ELISA Leishmania Microwell ELISA Kit Gnathostoma

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LIB	Device, General Purpose, Microbiology, Diagnostic	Microbiology	Class 1	866.2660	2026-06-01
GNH	Antigen, Fluorescent Antibody Test, Schistosoma Mansoni	Microbiology	Class 1	866.3600	2023-02-10
GPF	Antigen, Agglutinating, Echinococcus Spp.	Microbiology	Class 1	866.3200	2023-02-10
MDJ	Reagents, Cysticercosis	Microbiology	Class 1	866.3200	2023-02-10
MDT	Elisa, Trichinella Spiralis	Microbiology	Class 1	866.3850	2023-02-08
LOO	Reagent, Leishmanii Serological	Microbiology	Class 1	866.3870	2026-06-01
KHW	Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.	Microbiology	Class 2	866.3220	2023-02-10

Official Correspondent

David Lambillotte

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Eiger Diagnostics, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026241718. Last updated year: 2026. Please use registration number 3026241718 when referencing this establishment in official correspondence.