FDA applicant

Lone Star Technologies

Chatham, NJ2 decisions1998–19980 recalls

FDA records 2 decisions for Lone Star Technologies (Chatham, NJ) in 1998: 2 510(k) clearances. Most are in product codes EJB (Handle, Instrument, Dental) and ELW (Material, Impression). 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 Lone Star Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lone Star Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lone Star 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 “Lone”

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

Lone Star Medical Products, Inc. 6 Lone Star Trading Pte., Ltd. 1 Lone Oak Medical Technologies, LLC 1

Lone Star Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lone”