Data / Medical devices / Mattress, Air Flotation, Alternating Pressure

Mattress, Air Flotation, Alternating Pressure (FNM): 110 FDA-registered makers in 10 countries

110 establishments in 10 countries are registered with the FDA to make Mattress, Air Flotation, Alternating Pressure (product code FNM, Class 2, 21 CFR 880.5550). 0 of them have a 510(k) clearance or PMA approval on file and 5 have a recall event. The FDA has issued 102 510(k) clearances under this code, the latest on February 20, 1998, and lists 10 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

FNM

Device class

2

Regulation

880.5550

Medical specialty

General Hospital

Makers by country

Makers of Mattress, Air Flotation, Alternating Pressure

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 20, 1998. 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.