510(k) Report

FDA applicant

Bone Health Technologies, Inc.

Redwood City, CA1 decision2024–20240 recalls

FDA records 1 decision for Bone Health Technologies, Inc. (Redwood City, CA) in 2024: 1 De Novo grant. All are in product code QZO (Wearable Vibration Device For Orthopedic Use). 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, orthopedic panel, where it files most

How often FDA has decided Bone Health Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024: 1
2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Bone Health Technologies, Inc. by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Bone Health Technologies, 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 “Bone”

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