Data / Medical devices / Antisera, Fluorescent, Herpesvirus Hominis 1,2
Antisera, Fluorescent, Herpesvirus Hominis 1,2 (GQL): 5 FDA-registered makers in 2 countries
5 establishments in 2 countries are registered with the FDA to make Antisera, Fluorescent, Herpesvirus Hominis 1,2 (product code GQL, Class 2, 21 CFR 866.3305). 4 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 37 510(k) clearances under this code, the latest on August 28, 2009, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- GQL
- Device class
- 2
- Regulation
- 866.3305
- Medical specialty
- Microbiology
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| United Kingdom | 1 |
Makers of Antisera, Fluorescent, Herpesvirus Hominis 1,2
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Zeus Scientific LLC | Branchburg, NJ, United States | Manufacturer, Repackager or relabeler | 4 | November 7, 1991 | 0 | 0 | 0 | api.fda.gov |
| Diagnostic Automation/ Cortez Diagnostics Inc,. | Woodland Hills, CA, United States | Manufacturer | 2 | June 20, 1989 | 0 | 0 | 0 | api.fda.gov |
| Ortho-Clinical Diagnostics, Inc. | Athens, OH, United States | Complaint file establishment, Manufacturer | 1 | August 28, 2009 | 0 | 0 | 0 | api.fda.gov |
| Remel Europe Ltd | Dartford, Kent, United Kingdom | Manufacturer | 1 | December 13, 1990 | 0 | 0 | 0 | api.fda.gov |
| Immunocentrix Corporation | Canoga Park, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov |
Updated August 28, 2009. 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.