VMRD, Inc.

FDA Device Registration & Listing · FULLERTON, CA, US · Registration 3004036192

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004036192
FEI Number
3004036192
Entity Name
VMRD, Inc.
City/State/Country
FULLERTON, CA, US
Establishment Address
1312 E Valencia Dr, FULLERTON, CA 92831, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
VMRD, Inc. (Owner Number: 10092390)
Owner / Operator Contact Address
1312 E. Valencia Dr., Fullerton, CA 92831, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Orientia Spp. (Scrub Typhus) Serological Reagents - Orientia IgG MIF Assay; Orientia IgM MIF Assay Reagent, Rickettsia Serological - Rickettsia IgM ELISA Assay; Rickettsia typhi IgG ELISA; Rickettsia typhi IgM ELISA; SF Babesia Spp. Serological Reagents - Babesia IFA Test, Antigen, Nuclear, Epstein-Barr Virus - EBNA ACIF Slide Bartonella Spp. Serological Reagents - Bartonella IFA Immunofluorescent Assay, T. Cruzi - Trypanosoma IFA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QIQ Orientia Spp. (Scrub Typhus) Serological Reagents Unknown Class N N/A 2024-12-31
LSQ Reagent, Rickettsia Serological Microbiology Class 1 866.3500 2024-12-31
QIN Babesia Spp. Serological Reagents Unknown Class N N/A 2024-12-31
LLM Test, Antigen, Nuclear, Epstein-Barr Virus Microbiology Class 1 866.3235 2024-12-31
QIM Bartonella Spp. Serological Reagents Unknown Class N N/A 2024-12-31
MIV Immunofluorescent Assay, T. Cruzi Microbiology Class 1 866.3870 2024-12-31

Official Correspondent

Ethan Adams

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VMRD, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004036192. Last updated year: 2026. Please use registration number 3004036192 when referencing this establishment in official correspondence.
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