Data / Medical devices / Container, Specimen, Urine, Drugs Of Abuse, Over The Counter / United States
FDA-registered makers of Container, Specimen, Urine, Drugs Of Abuse, Over The Counter in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Container, Specimen, Urine, Drugs Of Abuse, Over The Counter (product code MPQ). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Container, Specimen, Urine, Drugs Of Abuse, Over The Counter
- Product code
- MPQ
- Country
- United States
Makers of Container, Specimen, Urine, Drugs Of Abuse, Over The Counter in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| American Plastics Co., Inc. | Glendale, AZ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomedical Polymers, Inc. | Sterling, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diagnostic Automation/ Cortez Diagnostics Inc,. | Woodland Hills, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ICON Injection Molding, Inc. | Phoenix, AZ, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mallinckrodt Manufacturing LLC | Madison, WI, United States | Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Omega Laboratories, Inc. | Mogadore, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Packaging Compliance Medical, LLC | Kentwood, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phamatech Inc. | San Diego, CA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Therapak, LLC | Oakwood, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Therapak, LLC | Claremont, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.