FDA applicant

Bloomfield Research and Development, Inc.

Hilton Head, SC3 decisions1986–19860 recalls

FDA records 3 decisions for Bloomfield Research and Development, Inc. (Hilton Head, SC) in 1986: 3 510(k) clearances. Most are in product codes ESE (Larynx, Artificial (Battery-Powered)) and DQD (Stethoscope, Electronic). 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, ear, nose and throat panel, where it files most

How often FDA has decided Bloomfield Research and Development, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bloomfield Research and Development, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Bloomfield Research and Development, Inc.

Which product codes does it file in?

What has FDA decided for it lately?