FDA applicant

Medi-Ked, Inc.

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Medi-Ked, Inc. (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code IQF (Orthosis, Cervical-Thoracic, Rigid). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Medi-Ked, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Medi-Ked”

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

Medi-Tech, Inc. 36 Medi-Globe Corp. 26 Medi-Flex Hospital Products, Inc. 13 Medi-Plast Intl., Inc. 12 The Medi-Dose Group 10 Medi Nuclear Corp., Inc. 9 Medi-Physics Inc. Dba Nycomed Amersham Imaging 9 Medi-Craft, Ltd. 9 Medi-Spec 8 Medi-Man Rehabilitation Products, Inc. 4 Medi Tex, Inc. 4 Medi-Dose, Inc. 4

Medi-Ked, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medi-Ked”