Data / Medical devices / United States / VMRD, Inc.
VMRD, Inc.: FDA-registered device maker in Fullerton, CA, United States, 1 510(k) clearance
VMRD, Inc. is registered with the FDA (registration 3004036192) in Fullerton, CA, United States. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 12, 1993. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004036192
- Address
- 1312 E Valencia Dr, Fullerton, CA, United States, 92831
- Owner or operator
- VMRD, Inc. (10092390)
- Roles
- Manufacturer, Manufacturer for export
- First device listed
- December 31, 2024
- Registered through
- 2026
- Brand names listed
- Anaplasma Spp. and Ehrlichia Spp. Serological Reagents - Anaplasma / Ehrlichia IFA, Antigen, Cf, Q Fever - Coxiella Burnetii MIF, Antigens, All, Leptospira Spp. - Leptospira IFA, Antigens, Slide and Tube, Francisella Tularensis - Francisella Tularensis IFA, Babesia Spp. Serological Reagents - Babesia IFA, Bartonella Spp. Serological Reagents - Bartonella IFA, Immunofluorescent Assay, T. Cruzi - Trypanosoma IFA, Orientia Spp. (Scrub Typhus) Serological Reagents - Orientia IgG MIF Assay; Orientia IgM MIF Assay and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Anaplasma Spp. And Ehrlichia Spp. Serological Reagents | QIO | N | Manufacturer for export | accessdata.fda.gov |
| Antigen, Cf, Q Fever | GPS | 1 | Manufacturer | accessdata.fda.gov |
| Antigens, All, Leptospira Spp. | GRY | 2 | Manufacturer for export | accessdata.fda.gov |
| Antigens, Slide And Tube, Francisella Tularensis | GSL | 2 | Manufacturer for export | accessdata.fda.gov |
| Babesia Spp. Serological Reagents | QIN | N | Manufacturer for export | accessdata.fda.gov |
| Bartonella Spp. Serological Reagents | QIM | N | Manufacturer for export | accessdata.fda.gov |
| Immunofluorescent Assay, T. Cruzi | MIV | 1 | Manufacturer for export | accessdata.fda.gov |
| Orientia Spp. (Scrub Typhus) Serological Reagents | QIQ | N | Manufacturer for export | accessdata.fda.gov |
| Reagent, Rickettsia Serological | LSQ | 1 | Manufacturer | accessdata.fda.gov |
| Test, Antigen, Nuclear, Epstein-Barr Virus | LLM | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 12, 1993 | K925690 | MERIDIAN EBNA TEST KIT | LLM | Substantially Equivalent | Fuller Laboratories, Inc. | accessdata.fda.gov |
Compare with other makers
Updated October 12, 1993. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.