510(k) Report

FDA applicant

Bemis Health Care

Mchenry, IL12 decisions1976–19890 recalls

FDA records 12 decisions for Bemis Health Care (Mchenry, IL) from 1976 to 1989: 12 510(k) clearances. Most are in product codes BYZ (Trap, Sterile Specimen) and FOB (Bedpan). 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 Bemis Health Care’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bemis Health Care since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Bemis”

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