FDA applicant

Zander Medical Supplies, Inc.

Vero Beach, FL5 decisions2000–20050 recalls

FDA records 5 decisions for Zander Medical Supplies, Inc. (Vero Beach, FL) from 2000 to 2005: 5 510(k) clearances. All are in product code MQG (Accessory, Assisted Reproduction). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Zander Medical Supplies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Zander Medical Supplies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Zander Medical Supplies, 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

Zander Medical Supplies, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?