FDA applicant

Barriermed Glove Co.

Lake Mary, FL5 decisions1999–20060 recalls

FDA records 5 decisions for Barriermed Glove Co. (Lake Mary, FL) from 1999 to 2006: 5 510(k) clearances. Most are in product codes KGO (Surgeon'S Gloves) and LZA (Polymer Patient Examination Glove). 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 and plastic surgery panel, where it files most

How often FDA has decided Barriermed Glove Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Barriermed Glove Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Barriermed Glove Co.’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 “Barriermed”

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

Barriermed, Inc. 3

Barriermed Glove Co.

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?

Other applicant names beginning “Barriermed”