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Data / Medical devices / Sling, Overhead Suspension, Wheelchair

Sling, Overhead Suspension, Wheelchair (INE): 16 FDA-registered makers in 5 countries

16 establishments in 5 countries are registered with the FDA to make Sling, Overhead Suspension, Wheelchair (product code INE, Class 1, 21 CFR 890.3910). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on January 24, 1989, and lists 0 recall events (0 Class I). FDA data exported November 3, 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
INE
Device class
1
Regulation
890.3910
Medical specialty
Physical Medicine

Makers by country

CountryMakers
United States7
China5
United Kingdom2
Canada1
Taiwan1

Makers of Sling, Overhead Suspension, Wheelchair

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
Alpha Modalities LLCFederal Way, WA, United StatesManufacturer0000api.fda.gov
Authority Medical GroupHillsboro, OR, United StatesManufacturer0000api.fda.gov
Blue Chip Medical Products, Inc.Suffern, NY, United StatesManufacturer0000api.fda.gov
Dongguan Vigor Textile Co.,LtdDongguan Guangdong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Emerald Resources IncNorth Syracuse, NY, United StatesSpecification developer0000api.fda.gov
Gbuk Group LimitedSelby North Yorkshire, United KingdomSpecification developer0000api.fda.gov
Hangzhou Rollmed Co.,ltd.Hangzhou Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Marketing Management & Associates Inc.Central City, NE, United StatesManufacturer0000api.fda.gov
Medco Technology LLCColumbia, SC, United StatesSpecification developer0000api.fda.gov
Metacare Industrial LtdGuangzhou Guangdong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Medtrica Solutions LtdSurrey British Columbia, CanadaContract manufacturer, Foreign private label distributor, Manufacturer0000api.fda.gov
Silvalea LtdNewton Abbot Devon, United KingdomManufacturer0000api.fda.gov
Span-America Medical Systems, Inc.Greenville, SC, United StatesContract manufacturer0000api.fda.gov
Suzhoushi Jasoncare Textiles Co., Ltdwujiang district, Suzhou Jiangsu, ChinaContract manufacturer0000api.fda.gov
Valentine Intl. Ltd.Hsichih City, Taipei Hsien, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Yearstar Healthcare Technology Co.,ltdJIANGYIN Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov

Updated January 24, 1989. 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.