Data / Medical devices / Humidifier, Non-Direct Patient Interface (Home-Use) / United States
FDA-registered makers of Humidifier, Non-Direct Patient Interface (Home-Use) in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Humidifier, Non-Direct Patient Interface (Home-Use) (product code KFZ). 1 has 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
- Humidifier, Non-Direct Patient Interface (Home-Use)
- Product code
- KFZ
- Country
- United States
Makers of Humidifier, Non-Direct Patient Interface (Home-Use) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Kaz USA, Inc., A Helen of Troy Company | Marlborough, MA, United States | Complaint file establishment, Specification developer | 1 | February 10, 1995 | 0 | 0 | 0 | api.fda.gov |
| Allied Medical LLC | Earth City, MO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bear Down Brands, LLC | Fullerton, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bio-Logic Aqua Research Technologies Int.. Inc | Grants Pass, OR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bruce Medical Supply | Waltham, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Crane Usa | Itasca, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Doner Industries, Inc. | Rogers, AR, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eng3 Corporation | Seattle, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lasko Products LLC | West Chester, PA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Michael Todd Beauty, LP | Port St Lucie, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sunbeam Products, Inc. | Atlanta, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vapore, LLC | Concord, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Westmed, Inc. | Tucson, AZ, United States | Contract manufacturer, Manufacturer, Specification developer | 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.