Levo Max

by Levo AG 510(k)

Active United States

510(k) K140706

Regulatory status

as of 27 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK140706	Date21 Jan 2015Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

510(k)

510(k) Number: K140706
FDA Product Code: ITI

Device Class: Class II
Regulation: 21 CFR Part 890.3860
Advisory Committee: Physical Medicine
FDA Decision: SESE Substantially Equivalent

Other devices from Levo AG

C3

Class I
Lcev

Class I
Levo Comfort Ii

Class II
Levo C3 Standup Wheelchair

Class II
Levo Combi

Class II
Summit EL

Class I

See all devices from Levo AG →