Data / Medical devices / Devices, Breath Trapping, Alcohol / United States
FDA-registered makers of Devices, Breath Trapping, Alcohol in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Devices, Breath Trapping, Alcohol (product code DJZ). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Devices, Breath Trapping, Alcohol
- Product code
- DJZ
- Country
- United States
Makers of Devices, Breath Trapping, Alcohol in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| KHN Solutions LLC | San Francisco, CA, United States | Complaint file establishment, Specification developer | 3 | March 24, 2009 | 0 | 0 | 0 | api.fda.gov |
| AlcoPro Inc | Knoxville, TN, United States | Manufacturer | 1 | April 6, 2011 | 0 | 0 | 0 | api.fda.gov |
| Germaine Laboratories, Inc. | San Antonio, TX, United States | Manufacturer, Repackager or relabeler | 1 | January 28, 2010 | 0 | 0 | 0 | api.fda.gov |
| Soberlink Healthcare LLC | Huntington Beach, CA, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | July 14, 2016 | 0 | 0 | 0 | api.fda.gov |
| Ak Globaltech Corp | Palisades Park, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alcopatrol Inc. | Houston, TX, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Consumer Safety Technology, LLC | Urbandale, IA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Express Manufacturing, Inc | Santa Ana, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lifeloc Technologies Inc | Wheat Ridge, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.