FDA applicant

Medical Flotation Systems, Inc.

Herndon, VA5 decisions1988–19890 recalls

FDA records 5 decisions for Medical Flotation Systems, Inc. (Herndon, VA) from 1988 to 1989: 5 510(k) clearances. Most are in product codes IOQ (Bed, Flotation Therapy, Powered) and LYG (Massager, Therapeutic, Manual). 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, physical medicine panel, where it files most

How often FDA has decided Medical Flotation Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Flotation Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Flotation Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?