510(k) Report

FDA applicant

Sensible Products

Santa Barbara, CA1 decision1993–19930 recalls

FDA records 1 decision for Sensible Products (Santa Barbara, CA) in 1993: 1 510(k) clearance. All are in product code FNL (Bed, Ac-Powered Adjustable Hospital). 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 Sensible Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sensible Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Sensible”

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