FDA applicant

Futura Medical Technology

Solana Beach, CA1 decision2002–20020 recalls

FDA records 1 decision for Futura Medical Technology (Solana Beach, CA) in 2002: 1 510(k) clearance. All are in product code MEG (Syringe, Antistick). 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, general hospital panel, where it files most

How often FDA has decided Futura Medical Technology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Futura Medical Technology since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Futura”

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

Futura Medical Developments Limited 1

Futura Medical Technology

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Futura”