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Data / Medical devices / Exerciser, Finger, Powered

Exerciser, Finger, Powered (JFA): 18 FDA-registered makers in 7 countries

18 establishments in 7 countries are registered with the FDA to make Exerciser, Finger, Powered (product code JFA, Class 1, 21 CFR 890.5410). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 12 510(k) clearances under this code, the latest on May 11, 1995, and lists 0 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.

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Product code
JFA
Device class
1
Regulation
890.5410
Medical specialty
Physical Medicine

Makers by country

CountryMakers
China8
United States5
United Kingdom1
Israel1
South Korea1
India1
Switzerland1

Makers of Exerciser, Finger, 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
Bioliberty LtdEdinburgh Edinburgh, City of, United KingdomSpecification developer0000api.fda.gov
Bo&bo LtdAmir Northern, IsraelSpecification developer0000api.fda.gov
Dynamic solution Co., LtdSeongnam-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Foshan Hongfeng Co.,ltdFoshan Guangdong, ChinaManufacturer0000api.fda.gov
Gizmospring.com Dongguan LimitedDongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Lantz MedicalMerrillville, IN, United StatesManufacturer0000api.fda.gov
MGRM Medicare Ltd.Khairatabad, Hyderabad Andhra Pradesh, IndiaManufacturer0000api.fda.gov
Motus NovaAtlanta, GA, United StatesManufacturer0000api.fda.gov
Ningbo Dericsson Smart Technology Co.,ltd.Ningbo City Zhejiang, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
NeuroXtherapeutics SALausanne Vaud, SwitzerlandComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Orthorpm Inc.Encinitas, CA, United StatesSpecification developer0000api.fda.gov
Shenzhen Sungpo Hi-Tech Electronic Co., LtdShenzhen Guangdong, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Shenzhen Willcareyou Technology Co., LtdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen XFT Medical LimitedShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Squegg IncPembroke Pines, FL, United StatesSpecification developer0000api.fda.gov
Tuper Medical Co., Ltd.Dezhou City Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Thuasne, LLCBakersfield, CA, United StatesContract manufacturer0000api.fda.gov
Zhejiang Todo Hardware Manufacture Co.,ltdJinhua Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov

Updated May 11, 1995. 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.