FDA applicant

T.A. Coleman Ent.

Washington, DC1 decision1998–19980 recalls

FDA records 1 decision for T.A. Coleman Ent. (Washington, DC) in 1998: 1 510(k) clearance. All are in product code EIA (Unit, Operative Dental). 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, dental panel, where it files most

How often FDA has decided T.A. Coleman Ent.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for T.A. Coleman Ent. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like T.A. Coleman Ent.’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

T.A. Coleman Ent.

Which product codes does it file in?

What has FDA decided for it lately?