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Data / Medical devices / Mattress, Flotation Therapy, Non-Powered / United Kingdom

FDA-registered makers of Mattress, Flotation Therapy, Non-Powered in the United Kingdom: 7 establishments

7 establishments in the United Kingdom are registered with the FDA to make Mattress, Flotation Therapy, Non-Powered (product code IKY). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Mattress, Flotation Therapy, Non-Powered
Product code
IKY
Country
United Kingdom

Makers of Mattress, Flotation Therapy, Non-Powered in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alpine HC Limited T/A Opera BedsHull Kingston upon Hull, City of, United KingdomSpecification developer0000api.fda.gov
Direct Healthcare Group Limited (THE KIRTON HEALTHCARE GROUP LTD)Caerphilly, United KingdomManufacturer0000api.fda.gov
Frontier Therapeutics LimitedTredegar Blaenau Gwent, United KingdomComplaint file establishment, Manufacturer0000api.fda.gov
Invacare UK Ltd.Bridgend, United KingdomManufacturer, Specification developer0000api.fda.gov
Jenx LimitedSheffield, United KingdomManufacturer0000api.fda.gov
Medstrom LtdCastle Donington Derby, United KingdomManufacturer0000api.fda.gov
Simple Stuff Works Associates LtdTamworth Staffordshire, United KingdomManufacturer0000api.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.