FDA applicant

The Medi-Dose Group

Feasterville, PA10 decisions1989–19950 recalls

FDA records 10 decisions for The Medi-Dose Group (Feasterville, PA) from 1989 to 1995: 10 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FMF (Syringe, Piston). 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 The Medi-Dose Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Medi-Dose Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Medi-Dose Group’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 “The”

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 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-Source, Inc. 4

The Medi-Dose Group

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”