FDA applicant

Medi-Stim Asa

Fridley, MN1 decision2010–20101 recall

FDA records 1 decision for Medi-Stim Asa (Fridley, MN) in 2010: 1 510(k) clearance. All are in product code DPW (Flowmeter, Blood, Cardiovascular). Its devices cite 2 predicates, 0 of them its own earlier devices. 1 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2010

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

1in 2025

2010high 1 (2025) · low 0 (2010)2026

Class I Class II/III not classified

FIG. 1 — Medi-Stim Asa by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medi-Stim Asa’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 “Medi-Stim”

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-Stim Asa

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Medi-Stim”