FDA applicant

Diabetes Sentry Products, LLC

Fort Worth1 decision1982–19820 recalls

FDA records 1 decision for Diabetes Sentry Products, LLC (Fort Worth) in 1982: 1 original PMA approval. All are in product code LMY (Monitor, Skin Resistance/Skin Temperature, For…). 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, general hospital panel, where it files most

How often FDA has decided Diabetes Sentry Products, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diabetes Sentry Products, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Diabetes Sentry Products, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Diabetes Sentry Products, LLC’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 “Diabetes”

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

Diabetes Technologies, Inc. 1 Diabetes Technologies, Inc. (Dti) 1

Diabetes Sentry Products, LLC

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Diabetes”