FDA applicant

Med-Tech Develoment Corp.

Clearwater, FL5 decisions1986–19860 recalls

FDA records 5 decisions for Med-Tech Develoment Corp. (Clearwater, FL) in 1986: 5 510(k) clearances. Most are in product codes HNN (Knife, Ophthalmic) and HHR (Laser, Surgical, Gynecologic). 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, ophthalmic panel, where it files most

How often FDA has decided Med-Tech Develoment Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med-Tech Develoment Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Med-Tech Develoment Corp.

Which product codes does it file in?

What has FDA decided for it lately?