FDA applicant

Anchor Brush Co., Inc.

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for Anchor Brush Co., Inc. (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code KDQ (Bottle, Collection, Vacuum). 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 hospital panel, where it files most

How often FDA has decided Anchor Brush Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anchor Brush Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Anchor Brush Co., 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 “Anchor”

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

Anchor Products Co. 7 Anchor Innovation Medical (A.I.M.) 2 Anchor Implants, Ltd. 2 Anchor Implant Systems, Inc. 1 Anchor Medical Technologies 1 Anchor Innovation Medical, Inc. 1

Anchor Brush Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Anchor”