FDA applicant

Garaventa Accessibility

Surrey, British Columbia, CA2 decisions2002–20040 recalls

FDA records 2 decisions for Garaventa Accessibility (Surrey, British Columbia, CA) from 2002 to 2004: 2 510(k) clearances. All are in product code ING (Elevator, Wheelchair, Portable). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Garaventa Accessibility since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Garaventa”

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

Garaventa (Canada), Ltd. 1 Garaventa (Canada) Ltd [Dba Garaventa Lift] 1

Garaventa Accessibility

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 “Garaventa”