FDA applicant

Pharmaseal Laboratories

Mchenry, IL5 decisions1976–19800 recalls

FDA records 5 decisions for Pharmaseal Laboratories (Mchenry, IL) from 1976 to 1980: 5 510(k) clearances. Most are in product codes KOZ (Beads, Hydrophilic, For Wound Exudate Absorption) and HHD (Pad, Menstrual, Unscented). 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 Pharmaseal Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pharmaseal Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pharmaseal Laboratories’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 “Pharmaseal”

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

Pharmaseal Div., Baxter Healthcare Corp. 24

Pharmaseal Laboratories

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pharmaseal”