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Data / Medical devices / Bed, Patient Rotation, Powered

Bed, Patient Rotation, Powered (IKZ): 18 FDA-registered makers in 6 countries

18 establishments in 6 countries are registered with the FDA to make Bed, Patient Rotation, Powered (product code IKZ, Class 2, 21 CFR 890.5225). 0 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 17 510(k) clearances under this code, the latest on February 20, 1998, and lists 10 recall events (0 Class I). FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get every maker of this deviceMakers in the United StatesWatch this device
Product code
IKZ
Device class
2
Regulation
890.5225
Medical specialty
Physical Medicine

Makers by country

CountryMakers
United States11
Canada2
India2
Taiwan1
United Kingdom1
China1

Makers of Bed, Patient Rotation, 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
Arjohuntleigh Magog, Inc.MAGOG Quebec, CanadaSpecification developer0010api.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
Carilex Medical, Inc.Guishan District Taoyuan, TaiwanManufacturer0000api.fda.gov
Encompass Group, LLC.McDonough, GA, United StatesSpecification developer0000api.fda.gov
Frontier Therapeutics LimitedTredegar Blaenau Gwent, United KingdomSpecification developer0000api.fda.gov
Geeken Seating Collection Private LimitedGURGAON Haryana, IndiaManufacturer0000api.fda.gov
Greens Surgicals Private LimitedVadodara Gujarat, IndiaManufacturer0000api.fda.gov
Kap MedicalCorona, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Kreg Medical, Inc.Melrose Park, IL, United StatesManufacturer0000api.fda.gov
Larand LLCNaperville, IL, United StatesManufacturer0000api.fda.gov
Ningbo Kangmailong Medical Apparatus Co.,LtdCixi City, Ningbo Zhejiang, ChinaManufacturer0000api.fda.gov
Probed Medical Technologies, Inc.ABBOTSFORD British Columbia, CanadaManufacturer0000api.fda.gov
Seneca Devices IncDurham, NC, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Stryker MedicalPortage, MI, United StatesComplaint file establishment, Manufacturer0010api.fda.gov
The Side Lyer CompanyOrlando, FL, United StatesManufacturer0000api.fda.gov
Turn Medical, LLCSan Antonio, TX, United StatesComplaint file establishment, Manufacturer0000api.fda.gov

Updated February 20, 1998. 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.