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Data / Medical devices / Bed, Ac-Powered Adjustable Hospital / United States

FDA-registered makers of Bed, Ac-Powered Adjustable Hospital in the United States: 37 establishments

37 establishments in the United States are registered with the FDA to make Bed, Ac-Powered Adjustable Hospital (product code FNL). 1 has a 510(k) clearance or PMA approval on file and 7 have a recall event. FDA data exported November 2, 2026.

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Device
Bed, Ac-Powered Adjustable Hospital
Product code
FNL
Country
United States

Makers of Bed, Ac-Powered Adjustable Hospital in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Stryker MedicalPortage, MI, United StatesComplaint file establishment, Manufacturer, Specification developer1December 16, 20100200api.fda.gov
Advanced Instrumentations, Inc.Miami, FL, United StatesManufacturer0000api.fda.gov
Agiliti Health - EllisEllis, KS, United StatesManufacturer0000api.fda.gov
Agiliti Health - HaysHays, KS, United StatesManufacturer0010api.fda.gov
Agiliti Health - MilwaukeeWauwatosa, WI, United StatesSpecification developer0000api.fda.gov
Beds By GeorgeElkhart, IN, United StatesManufacturer0000api.fda.gov
Caf Medical Solutions IncHockley, TX, United StatesManufacturer0000api.fda.gov
Crest Electronics Inc.Dassel, MN, United StatesManufacturer, Specification developer0000api.fda.gov
Curbell Medical Products, Inc.Orchard Park, NY, United StatesManufacturer, Specification developer0000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Emerald SupplyBrooklyn, NY, United StatesSpecification developer0000api.fda.gov
GF Health Products, Inc.Fond du Lac, WI, United StatesManufacturer0020api.fda.gov
Glory Medical Equipment, IncChino, CA, United StatesManufacturer0000api.fda.gov
Hard MFG. Co., Inc.Buffalo, NY, United StatesManufacturer0000api.fda.gov
Hill-Rom, Inc.Batesville, IN, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer00290api.fda.gov
Horst Enterprises IncSaint Petersburg, FL, United StatesSpecification developer0000api.fda.gov
Hosmed Inc.Doral, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
ICARE MEDICAL GROUP USA, IncGothenburg, NE, United StatesManufacturer0000api.fda.gov
Inovo Inc.Lehigh Acres, FL, United StatesManufacturer0000api.fda.gov
Joerns HealthcareCharlotte, NC, United StatesSpecification developer0000api.fda.gov
Joerns HealthcareArlington, TX, United StatesComplaint file establishment, Specification developer0010api.fda.gov
Kap MedicalCorona, CA, United StatesManufacturer0000api.fda.gov
Klyo Medical Systems IncDoral, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Kreg Medical, Inc.Melrose Park, IL, United StatesManufacturer0000api.fda.gov
Med-Mizer, IncBatesville, IN, United StatesManufacturer0020api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Metene LimitedCity of Industry, CA, United StatesSpecification developer0000api.fda.gov
Noa Medical IndustriesWashington, MO, United StatesManufacturer, Specification developer0000api.fda.gov
Opera Group IncNewark, NJ, United StatesSpecification developer0000api.fda.gov
Sleepsafe Beds, LLCBassett, VA, United StatesManufacturer0000api.fda.gov
The Morel CompanyBatesville, IN, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Tidi Products, LLCNeenah, WI, United StatesSpecification developer0000api.fda.gov
Us Med Equip, LLCHouston, TX, United StatesSpecification developer0000api.fda.gov
Vitalgo Inc.Miramar, FL, United StatesComplaint file establishment, Manufacturer0010api.fda.gov
Vivax Medical Corp.Naugatuck, CT, United StatesManufacturer0000api.fda.gov
Valmar Surgical Supplies, Inc.Lakewood, NJ, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
W.T. Farley, Inc.Ladson, SC, United StatesManufacturer0000api.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.