FDA applicant

Sherwood Medical Industries

Mchenry, IL62 decisions1976–19800 recalls

FDA records 62 decisions for Sherwood Medical Industries (Mchenry, IL) from 1976 to 1980: 62 510(k) clearances. Most are in product codes GIM (Tubes, Vacuum Sample, With Anticoagulant) and FYF (Cap, Surgical). 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, anesthesiology panel, where it files most

How often FDA has decided Sherwood Medical Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sherwood Medical Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sherwood Medical Industries’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 “Sherwood”

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

Sherwood Medical Co. 191

Sherwood Medical Industries

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 “Sherwood”