FDA applicant

Futuremed Div. of Future Impex Corp.

Deerpark, NY17 decisions1985–19940 recalls

FDA records 17 decisions for Futuremed Div. of Future Impex Corp. (Deerpark, NY) from 1985 to 1994: 17 510(k) clearances. Most are in product codes BZG (Spirometer, Diagnostic) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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, neurology panel, where it files most

How often FDA has decided Futuremed Div. of Future Impex Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Futuremed Div. of Future Impex Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Futuremed Div. of Future Impex Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Futuremed”

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

Futuremed America, Inc. 3

Futuremed Div. of Future Impex Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Futuremed”