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Data / Medical devices / Bed, Manual / United States

FDA-registered makers of Bed, Manual in the United States: 32 establishments

32 establishments in the United States are registered with the FDA to make Bed, Manual (product code FNJ). 0 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Get makers of this device in the United StatesWatch these makers
Device
Bed, Manual
Product code
FNJ
Country
United States

Makers of Bed, Manual in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abrams Nation, LLCGibsonia, PA, United StatesManufacturer0000api.fda.gov
Advanced Instrumentations, Inc.Miami, FL, United StatesManufacturer0000api.fda.gov
AKS Industries Inc.Scottsdale, AZ, United StatesManufacturer0000api.fda.gov
Alimed, LLCDedham, MA, United StatesSpecification developer0000api.fda.gov
Amenity Health, Inc.San Diego, CA, United StatesSpecification developer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Beds By GeorgeElkhart, IN, United StatesManufacturer0000api.fda.gov
Casco Manufacturing Solutions, Inc.Cincinnati, OH, United StatesManufacturer0000api.fda.gov
Crest Electronics Inc.Dassel, MN, United StatesSpecification developer0000api.fda.gov
Courtney Bed, IncBangor, ME, United StatesManufacturer0000api.fda.gov
Frontier Innovations, Inc.Vallejo, CA, United StatesSpecification developer0000api.fda.gov
GF Health Products, Inc.Fond du Lac, WI, United StatesManufacturer0000api.fda.gov
Halo Mobility Solutions LLCLas Vegas, NV, United StatesSpecification developer0000api.fda.gov
Hard MFG. Co., Inc.Buffalo, NY, United StatesManufacturer0000api.fda.gov
Helton IncMorrison, TN, United StatesContract manufacturer0000api.fda.gov
Hosmed Inc.Doral, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
ICARE MEDICAL GROUP USA, IncGothenburg, NE, United StatesManufacturer0000api.fda.gov
Innovative Products Unlimited, Inc.Niles, MI, United StatesManufacturer0000api.fda.gov
Joerns HealthcareArlington, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Klyo Medical Systems IncDoral, FL, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Lifeport, LLC.Woodland, WA, United StatesManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0011api.fda.gov
MJM International CorporationEdinburg, TX, United StatesManufacturer0000api.fda.gov
Mor-Medical InternationalPharr, TX, United StatesManufacturer0000api.fda.gov
NYOrthoBrooklyn, NY, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Pedicraft, Inc.Jacksonville, FL, United StatesManufacturer0000api.fda.gov
Radiation Products Design, Inc.Albertville, MN, United StatesManufacturer0000api.fda.gov
Skil-Care Corp.New Rochelle, NY, United StatesManufacturer0000api.fda.gov
Sleepsafe Beds, LLCBassett, VA, United StatesManufacturer0000api.fda.gov
Stryker MedicalPortage, MI, United StatesComplaint file establishment, Specification developer0010api.fda.gov
Tesla Biohealing, Inc.Milford, DE, United StatesManufacturer, Specification developer0000api.fda.gov
The Comfort Companies, L.L.C.New Berlin, WI, 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.