FDA applicant

Medtrek Corp.

Branford, CT1 decision1997–19970 recalls

FDA records 1 decision for Medtrek Corp. (Branford, CT) in 1997: 1 510(k) clearance. All are in product code ERL (Drill, Surgical, Ent (Electric Or Pneumatic)…). 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, ear, nose and throat panel, where it files most

How often FDA has decided Medtrek Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medtrek Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medtrek Corp.

Which product codes does it file in?

What has FDA decided for it lately?