FDA applicant

Convaid Products, Inc.

Mchenry, IL9 decisions1978–20170 recalls

FDA records 9 decisions for Convaid Products, Inc. (Mchenry, IL) from 1978 to 2017: 9 510(k) clearances. Most are in product codes IOR (Wheelchair, Mechanical) and LBE (Stroller, Adaptive). Its devices cite 4 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Convaid Products, LLC”.

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 Convaid Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2007high 1 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Convaid Products, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Convaid Products, Inc.’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 “Convaid”

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

Convaid, Ltd. 1 Convaid Product Development 1

Convaid Products, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Convaid”