Data / Medical devices / Drink, Glucose Tolerance
Drink, Glucose Tolerance (MRV): 6 FDA-registered makers in 1 country
6 establishments in 1 country are registered with the FDA to make Drink, Glucose Tolerance (product code MRV, Class 2, 21 CFR 862.1345). 3 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on June 21, 2012, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MRV
- Device class
- 2
- Regulation
- 862.1345
- Medical specialty
- Clinical Chemistry
Makers by country
| Country | Makers |
|---|---|
| United States | 6 |
Makers of Drink, Glucose Tolerance
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 |
|---|---|---|---|---|---|---|---|---|
| Azer Scientific, Inc. | Morgantown, PA, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | October 27, 2004 | 0 | 1 | 0 | api.fda.gov |
| Fisher Diagnostics | Middletown, VA, United States | Contract manufacturer, Manufacturer | 1 | November 18, 2003 | 0 | 0 | 0 | api.fda.gov |
| Vineland Syrup Inc. | Vineland, NJ, United States | Manufacturer | 1 | June 21, 2012 | 0 | 0 | 0 | api.fda.gov |
| Creative Essences Inc | Santa Fe Springs, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fresh Test, LLC | Los Angeles, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Products Laboratories, Inc. | Philadelphia, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated June 21, 2012. 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.