510(k) Report

FDA applicant

Happiest Baby, Inc.

Los Angeles, CA1 decision2023–20230 recalls

FDA records 1 decision for Happiest Baby, Inc. (Los Angeles, CA) in 2023: 1 De Novo grant. All are in product code QTG (Infant Supine Sleep System). 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 Happiest Baby, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2023: 1
2023high 1 (2023) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2023.

FIG. 1 — Happiest Baby, Inc. by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Happiest Baby, 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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