Data / Medical devices / Humidifier, Non-Direct Patient Interface (Home-Use)

Humidifier, Non-Direct Patient Interface (Home-Use) (KFZ): 91 FDA-registered makers in 13 countries

91 establishments in 13 countries are registered with the FDA to make Humidifier, Non-Direct Patient Interface (Home-Use) (product code KFZ, Class 1, 21 CFR 868.5460). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 20 510(k) clearances under this code, the latest on February 10, 1995, and lists 3 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

KFZ

Device class

1

Regulation

868.5460

Medical specialty

Anesthesiology

Makers by country

Makers of Humidifier, Non-Direct Patient Interface (Home-Use)

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.

Updated February 10, 1995. 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.