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Data / Medical devices / Bed, Flotation Therapy, Powered

Bed, Flotation Therapy, Powered (IOQ): 21 FDA-registered makers in 8 countries

21 establishments in 8 countries are registered with the FDA to make Bed, Flotation Therapy, Powered (product code IOQ, Class 2, 21 CFR 890.5170). 2 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 57 510(k) clearances under this code, the latest on March 10, 2015, and lists 21 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
IOQ
Device class
2
Regulation
890.5170
Medical specialty
Physical Medicine

Makers by country

CountryMakers
United States9
Dominican Republic2
Taiwan2
China2
Mexico2
Canada2
Czechia1
India1

Makers of Bed, Flotation Therapy, Powered

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.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Hill-Rom, Inc.Batesville, IN, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer2March 10, 2015020api.fda.gov
Numotech, Inc.Northridge, CA, United StatesSpecification developer1July 31, 1995000api.fda.gov
AccuMed Corp.Nigua San Cristobal, Dominican RepublicContract manufacturer0000api.fda.gov
Agiliti Health - CoronaCorona, CA, United StatesManufacturer0000api.fda.gov
Agiliti Health - EllisEllis, KS, United StatesManufacturer0000api.fda.gov
Agiliti Health - HaysHays, KS, United StatesManufacturer0000api.fda.gov
Arjo Dominican RepublicItabo, Haina San Cristobal, Dominican RepublicManufacturer0000api.fda.gov
Auxilium Medical, Inc.North Charleston, SC, United StatesManufacturer0000api.fda.gov
Carilex Medical, Inc.Guishan District Taoyuan, TaiwanManufacturer0000api.fda.gov
Grandrapids Foam Technologies, Inc.Grand Rapids, MI, United StatesContract manufacturer0000api.fda.gov
Guangdong Meicen Medical Equipment Co., Ltd.foshan Guangdong, ChinaManufacturer0000api.fda.gov
Hill-Rom De Mexico S De RL De CVAPODACA Nuevo Leon, MexicoContract manufacturer0000api.fda.gov
Kap MedicalCorona, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
LINET spol. s r.o.Slany Stredocesky Kraj, CzechiaManufacturer0000api.fda.gov
NPA de México S. de R.L. de C.V.TIJUANA Baja California, MexicoContract manufacturer0000api.fda.gov
Nureca Technologies Private LimitedMohali Punjab, IndiaManufacturer0000api.fda.gov
SHL Healthcare Ltd.SHENZHEN Guangdong, ChinaContract manufacturer0000api.fda.gov
Span Medical Products Canada ULCBEAMSVILLE Ontario, CanadaManufacturer0000api.fda.gov
Stryker MedicalPortage, MI, United StatesComplaint file establishment, Specification developer0020api.fda.gov
Umano Medical IncLevis Quebec, CanadaManufacturer0000api.fda.gov
Wellell Inc.New Taipei City, TaiwanContract manufacturer0000api.fda.gov

Updated March 10, 2015. 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.