FDA applicant

Mobius Mobility

Manchester, NH2 decisions2021–20251 recall

FDA records 2 decisions for Mobius Mobility (Manchester, NH) from 2021 to 2025: 2 510(k) clearances. All are in product code IMK (Wheelchair, Stair Climbing). Its devices cite 2 predicates, 1 of them its own earlier devices. 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Mobius Mobility’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

1in 2025

2021high 1 (2025) · low 0 (2021)2026

Class I Class II/III not classified

FIG. 1 — Mobius Mobility by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Mobius Mobility’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Mobius”

FDA records each applicant name separately; these may or may not be the same firm.

Mobius Imaging, LLC 3 Mobius Medical Systems, LP 3

Mobius Mobility

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Mobius”