FDA applicant

Molnlycke A/S Hospital Products

Mchenry, IL3 decisions1984–19860 recalls

FDA records 3 decisions for Molnlycke A/S Hospital Products (Mchenry, IL) from 1984 to 1986: 3 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and EFN (Cotton, Roll). 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 Molnlycke A/S Hospital Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Molnlycke A/S Hospital Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Molnlycke A/S Hospital Products by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Molnlycke A/S Hospital Products’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 “Molnlycke”

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

Molnlycke Health Care Us, LLC 27 Molnlycke Health Care, Inc. 19 Molnlycke/Scott Health Care 1 Molnlycke Health Care USA 1 Molnlycke Clinical Products AB 1

Molnlycke A/S Hospital Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Molnlycke”