Browse hierarchy: [Orthopedic (OR)](/submissions/OR) → [Subpart E — Surgical Devices](/submissions/OR/subpart-e%E2%80%94surgical-devices) → [21 CFR 888.5895](/submissions/OR/subpart-e%E2%80%94surgical-devices/888.5895) → QZO — Wearable Vibration Device For Orthopedic Use

# QZO · Wearable Vibration Device For Orthopedic Use

_Orthopedic · 21 CFR 888.5895 · Class 2_

**Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/QZO

## Overview

- **Product Code:** QZO
- **Device Name:** Wearable Vibration Device For Orthopedic Use
- **Regulation:** [21 CFR 888.5895](/submissions/OR/subpart-e%E2%80%94surgical-devices/888.5895)
- **Device Class:** 2
- **Review Panel:** [Orthopedic](/submissions/OR)

## Identification

The Osteoboost Belt is a wearable vibration device for orthopedic use, consisting of a vibration pack mounted to a nylon-covered neoprene belt. It is designed to transmit low-amplitude, high-frequency (20-40 Hz) mechanical vibrations to the spine and hips. It is indicated to reduce the decline in bone strength and volumetric bone density, as assessed via CT scans analyzed using the O.N. Diagnostics VirtuOst estimate, in postmenopausal women with osteopenia of the lumbar vertebrae or total hip as diagnosed via dual x-ray absorptiometry with a bone mineral density T-score between -1.0 and -2.49.

## Classification Rationale

Class II (special controls). The device is granted under De Novo classification (21 CFR 888.5895) as a wearable vibration device for orthopedic use, with risks mitigated by general and special controls.

## Special Controls

In combination with the general controls of the FD&C Act, the wearable vibration device for orthopedic use is subject to the following special controls:

## Recent Cleared Devices (1 of 1)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [DEN230015](https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/QZO/DEN230015.md) | Osteoboost Belt | Bone Health Technologies, Inc. | Jan 12, 2024 | DENG |

## Top Applicants

- Bone Health Technologies, Inc. — 1 clearance

---

**Source:** [https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/QZO](https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/QZO)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com