FDA applicant

Pride Mobility Product Corporration

Exeter, PA2 decisions2012–20122 recalls

FDA records 2 decisions for Pride Mobility Product Corporration (Exeter, PA) in 2012: 2 510(k) clearances. All are in product code ITI (Wheelchair, Powered). Its devices cite 2 predicates, 0 of them its own earlier devices. 2 recalls are 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 Pride Mobility Product Corporration’s devices, and how often a recall has named them.

FDA decisions per year

2in 2012

2012high 2 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

2in 2026

2012high 2 (2026) · low 0 (2012)2026

Class I Class II/III not classified

FIG. 1 — Pride Mobility Product Corporration by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Pride”

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

Pride Mobility Products Corp. 20 Pride Health Care, Inc. 19 Pride Health Care Equipment 2 Pride Mobility Product Corporation 1

Pride Mobility Product Corporration

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Pride”