FDA applicant

Medishield, Inc.

Mchenry, IL8 decisions1976–19780 recalls

FDA records 8 decisions for Medishield, Inc. (Mchenry, IL) from 1976 to 1978: 8 510(k) clearances. Most are in product codes HSN (Prosthesis, Ankle, Semi-Constrained, Cemented…) and DAT (Fibrinogen And Split Products, Peroxidase…). 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, orthopedic panel, where it files most

How often FDA has decided Medishield, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medishield, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medishield, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Medishield, Inc.

Which product codes does it file in?

What has FDA decided for it lately?