Ki

Little Wave Flip Manual Wheelchair

Registry build 21.09.26
1manufacturer
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Registered in Hebei. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LBE
Manufacturer City Province Registered as Device types
Imami Toys Hebei Co., Ltd. Handan Hebei Contract manufacturer 2

Record

Regulatory record for Ki
Listed by Ki Mobility, United States
FDA product code LBE
Device type Stroller, Adaptive
Device class Class 1
Regulation 21 CFR 890.3850
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K223533
Record published 2020-09-21
Record revised 2026-03-27 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Over the counter Yes
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Ki
Catalogue number Size Status
Little Wave Flip In distribution
Little Wave ARC In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Convaid Convaid Products LLC 46
Inspired by Drive Drive DeVilbiss Healthcare 7
Cruiser Convaid Products LLC 1
Safari Convaid Products LLC 1

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K223533 2023-08-31

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer