FDA applicant

Avery Intl.

Mentor, OH12 decisions1986–19870 recalls

FDA records 12 decisions for Avery Intl. (Mentor, OH) from 1986 to 1987: 12 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and KKX (Drape, Surgical, Antimicrobial). 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 Avery Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Avery Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Avery”

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

Avery Dennison Belgie Bvba 5 Avery Biomedical Devices, Inc. 2 Avery Dennison Medical, Ltd. 1 Avery Dennison Corporation 1

Avery Intl.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Avery”