FDA applicant

Pentron Laboratory Technologies

Wallingford, CT5 decisions2002–20030 recalls

FDA records 5 decisions for Pentron Laboratory Technologies (Wallingford, CT) from 2002 to 2003: 5 510(k) clearances. Most are in product codes EBF (Material, Tooth Shade, Resin) and EJH (Alloy, Metal, Base). Its devices cite 4 predicates, 0 of them its own earlier devices. 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 Pentron Laboratory Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pentron Laboratory Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pentron Laboratory Technologies’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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Other applicant names beginning “Pentron”

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

Pentron Corp. 15 Pentron Clinical Technologies 13 Pentron Clinical 4 Pentron Ceramics, Inc. 2

Pentron Laboratory Technologies

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Pentron”