FDA applicant

Nexus Health Care Products, Ltd.

Cobourg, Ontario, CA1 decision1991–19910 recalls

FDA records 1 decision for Nexus Health Care Products, Ltd. (Cobourg, Ontario, CA) in 1991: 1 510(k) clearance. All are in product code FPP (Stretcher, Hand-Carried). No 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, general hospital panel, where it files most

How often FDA has decided Nexus Health Care Products, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nexus Health Care Products, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Nexus Health Care Products, Ltd.’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 “Nexus”

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

Nexus Spine, LLC 19 Nexus Medical, LLC 16 Nexus Co., Ltd. C/O Yama Trans Co., Ltd. 3 Nexus CMF, LLC 3

Nexus Health Care Products, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nexus”