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Data / Medical devices / Stretcher, Wheeled, Powered

Stretcher, Wheeled, Powered (INK): 20 FDA-registered makers in 8 countries

20 establishments in 8 countries are registered with the FDA to make Stretcher, Wheeled, Powered (product code INK, Class 2, 21 CFR 890.3690). 3 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 12 510(k) clearances under this code, the latest on April 11, 2016, and lists 6 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
INK
Device class
2
Regulation
890.3690
Medical specialty
Physical Medicine

Makers by country

CountryMakers
United States7
China5
United Kingdom2
India2
Israel1
Taiwan1
Mexico1
Czechia1

Makers of Stretcher, Wheeled, 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
Champion MFG, INC.Ocala, FL, United StatesManufacturer2April 11, 2016000api.fda.gov
Savion Industries (1987), Ltd.ASHDOD Southern, IsraelManufacturer1September 28, 2005000api.fda.gov
Stryker MedicalPortage, MI, United StatesComplaint file establishment, Manufacturer, Specification developer1May 20, 2014060api.fda.gov
21ST Century Scientific, Inc.Coeur D Alene, ID, United StatesManufacturer0000api.fda.gov
Anetic Aid LtdHampshire England, United KingdomManufacturer0000api.fda.gov
Carevel Medical Systems Private LimitedGHAZIABAD Uttar Pradesh, IndiaManufacturer0000api.fda.gov
Dragon Medical Co.,LtdSuzhou City Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Fu Shun Hsing Technology Co., Ltd.Tainan City, TaiwanManufacturer0000api.fda.gov
Globus Medical, Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov
Hill-Rom De Mexico S De RL De CVAPODACA Nuevo Leon, MexicoContract manufacturer0000api.fda.gov
Hill-Rom, Inc.Batesville, IN, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Jac Custom PouchesDowagiac, MI, United StatesContract manufacturer0000api.fda.gov
Jiangsu Yongxin Medical Equipment Co., LtdZHANGJIAGANG Jiangsu, ChinaManufacturer0000api.fda.gov
Jiangyin Everise Medical Equipment Co., Ltd.Jiangyin Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
LINET spol. s r.o.Slany Stredocesky Kraj, CzechiaManufacturer0000api.fda.gov
Nuvasive, Inc.San Diego, CA, United StatesManufacturer0000api.fda.gov
Seers Medical LtdDebenham Suffolk, United KingdomContract manufacturer, Manufacturer0000api.fda.gov
United Surgical IndustriesSAHIBABAD Uttar Pradesh, IndiaManufacturer0000api.fda.gov
Yearstar Healthcare Technology Co.,ltdJIANGYIN Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Zhangjiagang New Fellow Med Co., Ltd.Zhangjiagang Jiangsu, ChinaManufacturer0000api.fda.gov

Updated April 11, 2016. 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.