Data / Medical devices / Canada / Kego Corporation

Kego Corporation: FDA-registered device maker in London Ontario, Canada, 1 510(k) clearance

Name: Kego Corporation FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Kego Corporation is registered with the FDA (registration 3008603863) in London Ontario, Canada. It lists 18 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 24, 2016. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3008603863
Address: 4350 Castleton Rd. Unit 3-4, London Ontario, Canada, N6N 0A3
Owner or operator: KEGO Corporation (10052258)
Roles: Exporter to the US
First device listed: July 6, 2016
Registered through: 2026
Brand names listed: ADAPTOR, GROOMING (MULTIPLE BRANDS), ADAPTOR, RECREATIONAL, MULTIPLE TYPES, BELT, WHEELCHAIR (MULTIPLE BRANDS), CANE CRUTCH HOLDERS, CANE WRIST STRAP, COMPONENTS; EXERCISE (MULTIPLE BRANDS), CPAPology, CVA SLING and more

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Wheelchair	KNO	1	Exporter to the US	accessdata.fda.gov
Adaptor, Dressing	ILD	1	Exporter to the US	accessdata.fda.gov
Adaptor, Grooming	ILW	1	Exporter to the US	accessdata.fda.gov
Adaptor, Hygiene	ILS	1	Exporter to the US	accessdata.fda.gov
Adaptor, Recreational	ILT	1	Exporter to the US	accessdata.fda.gov
Aid, Transfer	IKX	1	Exporter to the US	accessdata.fda.gov
Belt, Wheelchair	IQB	1	Exporter to the US	accessdata.fda.gov
Cable, Electrode	IKD	2	Exporter to the US	accessdata.fda.gov
Cable, Transducer And Electrode, Patient, (Including Connector)	DSA	2	Exporter to the US	accessdata.fda.gov
Cannula, Nasal, Oxygen	CAT	1	Exporter to the US	accessdata.fda.gov
Components, Exercise	IOD	1	Exporter to the US	accessdata.fda.gov
Device, Transfer, Patient, Manual	FMR	1	Exporter to the US	accessdata.fda.gov
Holder, Crutch And Cane, Wheelchair	IMZ	1	Exporter to the US	accessdata.fda.gov
Sling, Arm	ILI	1	Exporter to the US	accessdata.fda.gov
Strap, Head, Gas Mask	BTK	1	Exporter to the US	accessdata.fda.gov
Tubing, Pressure And Accessories	BYX	1	Exporter to the US	accessdata.fda.gov
Utensil, Eating	ILC	1	Exporter to the US	accessdata.fda.gov
Utensil, Homemaking	IKW	1	Exporter to the US	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
October 24, 2016	K153188	Caremed patient cable and leadwires	DSA	Substantially Equivalent	Shenzhen Caremed Medical Technology Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated October 24, 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.