510(k) Report

FDA applicant

Trebay Medical Corp.

Clearwater, FL14 decisions1995–19960 recalls

FDA records 14 decisions for Trebay Medical Corp. (Clearwater, FL) from 1995 to 1996: 14 510(k) clearances. Most are in product codes EQJ (Bur, Ear, Nose And Throat) and 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 Trebay Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trebay Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Trebay Medical 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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