510(k) Report

FDA applicant

Sweet Dreams, Inc.

Worthington, OH1 decision1986–19860 recalls

FDA records 1 decision for Sweet Dreams, Inc. (Worthington, OH) in 1986: 1 510(k) clearance. All are in product code FMS (Bed, Pediatric Open 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 Sweet Dreams, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sweet Dreams, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sweet Dreams, 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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Other applicant names beginning “Sweet”

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