FDA applicant

The Myerson Company Limited

Laventille, TT2 decisions2017–20230 recalls

FDA records 2 decisions for The Myerson Company Limited (Laventille, TT) from 2017 to 2023: 2 510(k) clearances. All are in product code EBI (Resin, Denture, Relining, Repairing, Rebasing). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Myerson, LLC”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided The Myerson Company Limited’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — The Myerson Company Limited by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like The Myerson Company Limited’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “The”

FDA records each applicant name separately; these may or may not be the same firm.

Myerson Tooth Corp. 2

The Myerson Company Limited

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “The”