Data / Medical devices / Antisera, All Types, Shigella Spp.
Antisera, All Types, Shigella Spp. (GNB): 5 FDA-registered makers in 4 countries
5 establishments in 4 countries are registered with the FDA to make Antisera, All Types, Shigella Spp. (product code GNB, Class 2, 21 CFR 866.3660). 1 of them has a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 41 510(k) clearances under this code, the latest on May 31, 1996, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- GNB
- Device class
- 2
- Regulation
- 866.3660
- Medical specialty
- Microbiology
Makers by country
| Country | Makers |
|---|---|
| United States | 2 |
| United Kingdom | 1 |
| Mexico | 1 |
| China | 1 |
Makers of Antisera, All Types, Shigella Spp.
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 |
|---|---|---|---|---|---|---|---|---|
| Remel Europe Ltd | Dartford, Kent, United Kingdom | Manufacturer | 1 | January 11, 1990 | 0 | 0 | 0 | api.fda.gov |
| Becton, Dickinson & Co. | Sparks, MD, United States | Complaint file establishment, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Biomerica De Mexico, S.A. De C.V. | MEXICALI Baja California, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lee Laboratories, Inc. | Grayson, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Tianlong Biotechnology Co., Ltd. | Suzhou Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated May 31, 1996. 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.