FDA applicant

Medi-Man Rehabilitation Products, Inc.

Canada, L4w 1p4, CA4 decisions1985–20000 recalls

FDA records 4 decisions for Medi-Man Rehabilitation Products, Inc. (Canada, L4w 1p4, CA) from 1985 to 2000: 4 510(k) clearances. Most are in product codes ILJ (Bath, Hydro-Massage) and INQ (Table, Powered). 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-Man Rehabilitation Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medi-Man Rehabilitation Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medi-Man Rehabilitation Products, 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-Man”

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 Tex, Inc. 4 Medi-Dose, Inc. 4 Medi-Source, Inc. 4

Medi-Man Rehabilitation Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medi-Man”