FDA applicant

Beacon Laboratories, Inc.

Broomfield, CO18 decisions1989–19940 recalls

FDA records 18 decisions for Beacon Laboratories, Inc. (Broomfield, CO) from 1989 to 1994: 18 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and HAM (Apparatus, Electrosurgical). 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 Beacon Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Beacon Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Beacon Laboratories, Inc.’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 “Beacon”

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

Beacon Biosignals, Inc. 4 Beacon Converters, Inc. 2 Beacon Surgical, Inc. 2 Beacon Biologicals, Inc. 1 Beacon Endoscopic 1

Beacon Laboratories, 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?

Other applicant names beginning “Beacon”