510(k) Report

FDA applicant

Custom Hospitals Products

Portland, OR1 decision1989–19890 recalls

FDA records 1 decision for Custom Hospitals Products (Portland, OR) in 1989: 1 510(k) clearance. All are in product code KMO (Binder, Elastic). 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 Custom Hospitals Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Custom Hospitals Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Custom Hospitals 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 “Custom”

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