510(k) Report

FDA applicant

Medical Technology Development Corp.

Clearwater, FL5 decisions1986–19940 recalls

FDA records 5 decisions for Medical Technology Development Corp. (Clearwater, FL) from 1986 to 1994: 5 510(k) clearances. Most are in product codes HNN (Knife, Ophthalmic) and EZL (Catheter, Retention Type, Balloon). 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 Medical Technology Development Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Technology Development Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Technology Development Corp.’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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