FDA applicant

Avery Dennison Belgie Bvba

Turnhout, BE5 decisions2012–20210 recalls

FDA records 5 decisions for Avery Dennison Belgie Bvba (Turnhout, BE) from 2012 to 2021: 5 510(k) clearances. Most are in product codes FRO (Dressing, Wound, Drug) and KKX (Drape, Surgical, Antimicrobial). Its devices cite 4 predicates, 3 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 Avery Dennison Belgie Bvba’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Avery Dennison Belgie Bvba by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Avery Dennison Belgie Bvba’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 “Avery”

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

Avery Intl. 12 Avery Biomedical Devices, Inc. 2 Avery Dennison Medical, Ltd. 1 Avery Dennison Corporation 1

Avery Dennison Belgie Bvba

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Avery”