510(k) Report

FDA applicant

Diabetic Supply of Suncoast, Inc.

Dorado, PR1 decision2016–20160 recalls

FDA records 1 decision for Diabetic Supply of Suncoast, Inc. (Dorado, PR) in 2016: 1 510(k) clearance. All are in product code FMI (Needle, Hypodermic, Single Lumen). Its devices cite 1 predicate, 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, general hospital panel, where it files most

How often FDA has decided Diabetic Supply of Suncoast, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016: 1
2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Diabetic Supply of Suncoast, Inc. by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • FMINeedle, Hypodermic, Single Lumen1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K160199Advocate Insulin Pen NeedlesDiabetic Supply of Suncoast, Inc. · 2016

The one decision as Diabetic Supply of Suncoast, Inc. →