FDA applicant

Mcneil Healthcare, Inc.

Waterford, CT19 decisions1994–19940 recalls

FDA records 19 decisions for Mcneil Healthcare, Inc. (Waterford, CT) in 1994: 19 510(k) clearances. Most are in product codes EFQ (Gauze/Sponge, Internal) and GDY (Gauze/Sponge, Internal, X-Ray Detectable). 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 Mcneil Healthcare, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mcneil Healthcare, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Mcneil”

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

Mcneil-Ppc, Inc. 6

Mcneil Healthcare, 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 “Mcneil”