FDA applicant

Futuremed America, Inc.

Chatsworth, CA3 decisions1995–19980 recalls

FDA records 3 decisions for Futuremed America, Inc. (Chatsworth, CA) from 1995 to 1998: 3 510(k) clearances. All are in product code BZG (Spirometer, Diagnostic). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Futuremed America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Futuremed America, Inc. 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 Div. of Future Impex Corp. 17

Futuremed America, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Futuremed”