FDA applicant

Guardian Angel Products, Inc.

Washington, DC5 decisions1990–20030 recalls

FDA records 5 decisions for Guardian Angel Products, Inc. (Washington, DC) from 1990 to 2003: 5 510(k) clearances. Most are in product codes DRL (Tester, Defibrillator) and GDF (Guide, Needle, Surgical). Its devices cite 1 predicate, 1 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, general and plastic surgery panel, where it files most

How often FDA has decided Guardian Angel Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Guardian Angel Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Guardian Angel 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 “Guardian”

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

Guardian Products Co., Inc. 8 Guardian Scientific, Corp. 4 Guardian Group, Inc. 2 Guardian Chemical 2

Guardian Angel Products, Inc.

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Guardian”