FDA applicant

Oxboro Medical Intl., Inc.

Ham Lake, MN6 decisions1988–19961 recall

FDA records 6 decisions for Oxboro Medical Intl., Inc. (Ham Lake, MN) from 1988 to 1996: 6 510(k) clearances. Most are in product codes KCT (Sterilization Wrap Containers, Trays…) and GDX (Scalpel, One-Piece). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Oxboro Medical Intl., Inc. since 2007.

Recalls per year

1in 2013

2007high 1 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

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Oxboro Medical Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?