510(k) Report

FDA applicant

Replacement Parts Industries, Inc.

Chatsworth, CA3 decisions2002–20020 recalls

FDA records 3 decisions for Replacement Parts Industries, Inc. (Chatsworth, CA) in 2002: 3 510(k) clearances. Most are in product codes FMT (Warmer, Infant Radiant) and LBI (Unit, Neonatal Phototherapy). Its devices cite 13 predicates, 0 of them its own earlier 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 Replacement Parts Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Replacement Parts Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Replacement Parts Industries, 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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