FDA applicant

Ansell Perry

Massillon, OH22 decisions1997–200110 recalls

FDA records 22 decisions for Ansell Perry (Massillon, OH) from 1997 to 2001: 22 510(k) clearances. Most are in product codes KGO (Surgeon'S Gloves) and LYY (Latex Patient Examination Glove). 10 recalls are 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 Ansell Perry’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ansell Perry since 2007.

Recalls per year

1in 2016

2007high 8 (2009) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Ansell”

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

Ansell Healthcare Products, LLC 36 Ansell, Inc. 30 Ansell Intl. 4 Ansell Healthcare, Inc. 3 Ansell Edmont Industrial, Inc. 2 Ansell Pacific, Inc. 2 Ansell Heathcare Products, LLC 1 Ansell Malaysia Sdn Bhd 1

Ansell Perry

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?

What has been recalled?

Other applicant names beginning “Ansell”