Data / Medical devices / United States / Viro Research LLC
Viro Research LLC: FDA-registered device maker in Snellville, GA, United States, 1 510(k) clearance
Viro Research LLC is registered with the FDA (registration 3016467093) in Snellville, GA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 15, 1994. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3016467093
- Address
- 2326 Wisteria Drive #220, Snellville, GA, United States, 30078
- Owner or operator
- Viro Research LLC (10062481)
- Roles
- Manufacturer
- First device listed
- January 31, 2020
- Registered through
- 2027
- Brand names listed
- Zostergent VZV Identification Reagent
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Antigen, Cf, (Including Cf Control), Varicella-Zoster | GQW | 2 | 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 |
|---|---|---|---|---|---|---|
| December 15, 1994 | K942743 | VIRO VARICELLA-ZOSTER VIRUS IDENTIFICATION REAGENT | GQW | Substantially Equivalent | Viro Research, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 15, 1994. 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.