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

FDA-registered makers of Mattress, Air Flotation, Alternating Pressure in the United States: 35 establishments

35 establishments in the United States are registered with the FDA to make Mattress, Air Flotation, Alternating Pressure (product code FNM). 0 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 3, 2026.

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Device
Mattress, Air Flotation, Alternating Pressure
Product code
FNM
Country
United States

Makers of Mattress, Air Flotation, Alternating Pressure in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alpha TeknikoLake Zurich, IL, United StatesManufacturer0000api.fda.gov
Agiliti Health - CoronaCorona, CA, United StatesContract manufacturer, Manufacturer0010api.fda.gov
Agiliti Health - EllisEllis, KS, United StatesComplaint file establishment, Manufacturer0010api.fda.gov
Agiliti Health - HaysHays, KS, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Agiliti Health - MilwaukeeWauwatosa, WI, United StatesSpecification developer0000api.fda.gov
Blue Chip Medical Products, Inc.Suffern, NY, United StatesManufacturer0000api.fda.gov
Brace AlignSoddy Daisy, TN, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Compass Health Brands (distribution Center)Brook Park, OH, United StatesManufacturer0000api.fda.gov
Cross Innovations LLCCheyenne, WY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Custom Medical SolutionsMinneapolis, MN, United StatesManufacturer0000api.fda.gov
Drive Northpoint, LLCPalmetto, GA, United StatesManufacturer0000api.fda.gov
Encompass Group, LLC.McDonough, GA, United StatesSpecification developer0000api.fda.gov
Emerald SupplyBrooklyn, NY, United StatesSpecification developer0000api.fda.gov
Genadyne Biotechnologies, Inc.Hicksville, NY, United StatesManufacturer0000api.fda.gov
Great Life HealthcareArcadia, CA, United StatesManufacturer0000api.fda.gov
Immersus Health Company, LLCMilford, OH, United StatesSpecification developer0000api.fda.gov
Joerns HealthcareCharlotte, NC, United StatesSpecification developer0000api.fda.gov
Joerns HealthcareArlington, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Joerns Healthcare BrownsvilleBrownsville, TX, United StatesManufacturer0000api.fda.gov
Kap MedicalCorona, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Kreg Medical, Inc.Melrose Park, IL, United StatesManufacturer0000api.fda.gov
Levisense Medical, Inc.Beverly, MA, United StatesSpecification developer0000api.fda.gov
Med Way Inc.Buford, GA, United StatesManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Mizuho Orthopedic Systems, Inc.Union City, CA, United StatesManufacturer0000api.fda.gov
Moxi Enterprises, LLCGreenville, SC, United StatesContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Nova Ortho-Med, Inc.North Aurora, IL, United StatesSpecification developer0000api.fda.gov
Obbomed Group LLCPomona, CA, United StatesSpecification developer0000api.fda.gov
Richardson Products, Inc.Frankfort, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Rogers Foam CorporationMt Sterling, KY, United StatesContract manufacturer0000api.fda.gov
Span-America Medical Systems, Inc.Greenville, SC, United StatesManufacturer, Specification developer0000api.fda.gov
Stryker MedicalPortage, MI, United StatesComplaint file establishment, Manufacturer, Specification developer0020api.fda.gov
Thin Air Surfaces, LLCWahpeton, ND, United StatesSpecification developer0000api.fda.gov
Turncare, Inc.Pompton Plains, NJ, United StatesManufacturer0020api.fda.gov
WCW,IncManchester Center, VT, United StatesContract manufacturer, Manufacturer0000api.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.