Data / Medical devices / Enzyme Linked Immunosorbent Assay, Coccidioides Immitis
Enzyme Linked Immunosorbent Assay, Coccidioides Immitis (MIY): 4 FDA-registered makers in 1 country
4 establishments in 1 country are registered with the FDA to make Enzyme Linked Immunosorbent Assay, Coccidioides Immitis (product code MIY, Class 2, 21 CFR 866.3135). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on July 10, 1992, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MIY
- Device class
- 2
- Regulation
- 866.3135
- Medical specialty
- Microbiology
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
Makers of Enzyme Linked Immunosorbent Assay, Coccidioides Immitis
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 |
|---|---|---|---|---|---|---|---|---|
| Meridian Bioscience, Inc. | Cincinnati, OH, United States | Manufacturer | 1 | July 10, 1992 | 0 | 0 | 0 | api.fda.gov |
| Cactus Bio, LLC | Phoenix, AZ, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| IMMY, Inc. | Norman, OK, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lumiquick Diagnostics, Inc. | Santa Clara, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated July 10, 1992. 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.