510(k) Report

FDA applicant

Maril Products, Inc.

Tustin, CA2 decisions1995–19990 recalls

FDA records 2 decisions for Maril Products, Inc. (Tustin, CA) from 1995 to 1999: 2 510(k) clearances. All are in product code LRJ (Disinfectant, Medical Devices). 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 Maril Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Maril Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Maril Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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