510(k) Report

FDA applicant

Hf Scientific, Inc.

Ft. Myers, FL5 decisions1987–19880 recalls

FDA records 5 decisions for Hf Scientific, Inc. (Ft. Myers, FL) from 1987 to 1988: 5 510(k) clearances. Most are in product codes CIE (Volumetric/Manometric, Carbon-Dioxide) and JGS (Electrode, Ion Specific, Sodium). 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, clinical chemistry panel, where it files most

How often FDA has decided Hf Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hf Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hf Scientific, Inc.’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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