FDA-cleared
Osteoboost received FDA De Novo clearance as a Class II device and Breakthrough status for providing a more effective treatment for osteopenia.
Clinically proven
Osteoboost was tested in a randomized, double-blind, sham-controlled trial and demonstrated significant reductions in bone loss.
No device-related serious adverse events
In the clinical trial, side effects were typically mild to moderate, transient, and resolved after temporarily stopping use.
High patient adherence
Study completers averaged 4.1 weekly sessions with 82% adherence. Participants rated it 8/10 for ease of fitting in 5 weekly sessions.

Advancing bone health through a gold-standard pivotal trial

Osteoboost was tested in a randomized, double-blind, sham-controlled trial—the highest standard in research—and showed significant reductions in bone loss.

85% reduction in vertebral bone density loss

Participants who used Osteoboost at least 3 times per week saw an 85% reduction in loss of vertebral bone density after 12 months, compared to the placebo group.
Graph showing that participants who used Osteoboost at least 3 times per week saw an 85% reduction in loss of vertebral bone density after 12 months, compared to the placebo group.

83% reduction in vertebral bone strength loss

Participants who used Osteoboost at least 3 times per week saw an 83% reduction in loss of vertebral bone strength after 12 months, compared to the placebo group.
Graph showing that participants who used Osteoboost at least 3 times per week saw an 83% reduction in loss of vertebral bone strength after 12 months, compared to the placebo group.

55% reduction in hip bone density loss

Participants who used Osteoboost at least 3 times per week saw a 55% reduction in loss of hip bone density after 12 months, compared to the placebo group.
Graph showing that participants who used Osteoboost at least 3 times per week saw a 55% reduction in loss of hip bone density after 12 months, compared to the placebo group.

Simple by design, calibrated for precision

Osteoboost delivers calibrated mechanical stimulation to the lumbar spine and hips, mimicking the benefits of high-impact exercise.

Put on the device

The patient wraps Osteoboost low around the hips, positioning the vibration pack snugly over the sacrum. A force sensor ensures correct contact to support precise delivery of therapy.

Stand still for automated calibration

Once secured, Osteoboost uses embedded sensors to measure vibration at the iliac crest and automatically adjusts output to deliver a calibrated therapeutic dose (0.1–0.3 g at 20–40 Hz).

Wear during daily activity

Each 30-minute session provides targeted sinusoidal vibration to the lumbar spine and hips. Patients can walk or perform light tasks while the therapy runs, supporting consistent adherence without interfering with daily life.

How to prescribe Osteoboost

Osteoboost is a Class II prescription device, currently available as self-pay. No prior authorization or in-office setup required.
Step 1

Identify patient with low bone density

Osteoboost is FDA-cleared for postmenopausal women diagnosed with osteopenia (T-score -1.0 to -2.49), providing a safe, effective, and convenient non-drug treatment to help reduce bone loss.
Step 2

Submit prescription to our partner pharmacy

Fax, call, or e-prescribe to HealthWarehouse:

Fax: 1-888-870-2808
Phone: 1-800-748-7001
E-Prescribe: NPI: 1619252160; NCPDP#: 1832674
Step 3

Instruct patient to order and pay online

Patients must complete their purchase at our website. Both a prescription and order are required for shipment. The device is currently self-pay, and we’re actively working toward reimbursement.

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