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Data / Medical devices / Dynamometer, Ac-Powered

Dynamometer, Ac-Powered (LBB): 15 FDA-registered makers in 10 countries

15 establishments in 10 countries are registered with the FDA to make Dynamometer, Ac-Powered (product code LBB, Class 2, 21 CFR 888.1240). 2 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 36 510(k) clearances under this code, the latest on March 9, 2017, and lists 1 recall event (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
LBB
Device class
2
Regulation
888.1240
Medical specialty
Orthopedic

Makers by country

CountryMakers
United States4
South Korea2
China2
Israel1
United Kingdom1
France1
Greece1
Canada1
Belgium1
Australia1

Makers of Dynamometer, Ac-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
Hoggan Scientific LLCSalt Lake City, UT, United StatesManufacturer1March 9, 2017000api.fda.gov
Saehan CorporationChangwon Gyeongnam, South KoreaManufacturer1September 27, 2005000api.fda.gov
ActivbodySan Diego, CA, United StatesComplaint file establishment, Specification developer0010api.fda.gov
Bo&bo LtdAmir Northern, IsraelSpecification developer0000api.fda.gov
Eforto Health IncNew York, NY, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Gripable LtdBeaconsfield Buckinghamshire, United KingdomComplaint file establishment, Specification developer0000api.fda.gov
InBody Co, Ltd.Cheonan-si Chungnam, South KoreaManufacturer0000api.fda.gov
Kinvent BiomecaniqueMontepellier Herault, FranceManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Kinvent HellasThermi Kentriki Makedonia, GreeceManufacturer, Remanufacturer0000api.fda.gov
Kube Innovation Inc.Montreal Quebec, CanadaComplaint file establishment, Manufacturer0000api.fda.gov
Suga Electronics (dongguan) Co. Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Suga Technology (dongguan) Co.. Ltd.Dongguan Guangdong, ChinaContract manufacturer0000api.fda.gov
Squegg IncPembroke Pines, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
UniWeb BVMeise Vlaams Brabant, BelgiumComplaint file establishment, Manufacturer0000api.fda.gov
Vald Performance (usa) Pty LtdNewstead Queensland, AustraliaComplaint file establishment, Manufacturer, Remanufacturer0000api.fda.gov

Updated March 9, 2017. 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.