FDA applicant

Mdt Corp., Inc.

Rochester, NY22 decisions1979–19960 recalls

FDA records 22 decisions for Mdt Corp., Inc. (Rochester, NY) from 1979 to 1996: 22 510(k) clearances. Most are in product codes FRC (Indicator, Biological Sterilization Process) and GDC (Table, Operating-Room, Electrical). Its devices cite 3 predicates, 2 of them its own earlier devices. 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 Mdt Corp., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mdt Corp., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mdt Corp., Inc.’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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Mdt Corp., Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?