
Wesper Lab
Airflow data. No cannula. No compromise.
- Airflow
- Thoracic effort
- Abdominal effort
- Pressure
- Body position
- SpO2
- PPG
- Heart rate
- Sleep staging
95%+AHI correlation to PSG
Wesper Lab
FDA-Cleared Home Sleep Testing
Two levels of FDA-cleared home sleep testing on one clinical workflow. Match the right test to every patient while Wesper handles the logistics around it.

AHI correlation to in-lab PSG
Featured In

The Access Gap
About 80% of people with obstructive sleep apnea haven't been diagnosed. Getting each patient tested takes devices, shipping, follow-up and scoring, and that work adds up for a busy clinic. Wesper takes it on so more patients can be tested.
84M
Americans estimated to have obstructive sleep apnea
80%
of cases estimated to be undiagnosed
45,000
Americans for every board-certified sleep physician (about 7,500 nationwide)
AASM; U.S. Census Bureau
Scalable Solution
Wesper Lab and Wesper Lite share one portal, one patient record and one interpretation pipeline. Start where the patient is, and escalate without re-onboarding.

Airflow data. No cannula. No compromise.
95%+AHI correlation to PSG
Wesper Lab
Light. Compact. High clinical confidence.
95%+AHI correlation to PSG
Wesper LiteIndicated for adult use only.
How It Works
You order the test and make the clinical decisions. Wesper handles shipping, patient support and scoring, and results come back to your team.
One click from the Wesper portal or your EMR.
Devices go straight to the patient's door, with return shipping included.
Automated reminders, prep and check-ins, backed by 24/7 patient support.
Multi-night testing comes standard with every Wesper study.
Automatic scoring with full access to raw data for clinician review. Optional access to board-certified sleep physicians in all 50 states.
Re-test over time on the same patient record to see whether treatment is working.
Evidence
Wesper has been studied against in-lab polysomnography and against clinicians' own scoring. The source for each result is listed with it.
95%+
AHI correlation to in-lab PSG
Sleep Medicine 2025; JCSM 2023
r = 0.98
Automatic scoring vs. provider manual scoring
Sleep Medicine 2026
<5 days
From order to successful test
Wesper, Q3 2026
99%+
Patient success rate
Wesper, Q3 2026
TIME Best Inventions of 2026, Special Mention. Read the announcement
The Wesper Portal
Each study opens in the Wesper portal with full access to the raw data, so your clinicians can check the automatic scoring and compare results with earlier nights. Reports go out with your clinic's branding.

99%+patient success rate
For Patients
Cannula-free sensors, guided setup in the app and 24/7 support help patients test at home, in their own bed, over more than one night. If anything feels off during setup, our support team is there to help.
Who We Work With
Wesper works with practices of every size that care for patients with sleep-disordered breathing.
Direct respiratory data, multi-night studies and full access to raw data for reads you can defend.
For sleep clinicsScale home testing across service lines, with EMR integration and SOC 2 Type 2 security.
For health systemsOrder a sleep test like any other lab, and connect to a board-certified sleep physician for interpretation.
For primary careTest before surgery and follow patients over time on one record.
For bariatric programsTrack sleep apnea over time as patients progress through GLP-1 therapy.
For GLP-1 programsTest more patients with the staff you have. Dropship, patient support and scoring are handled for you.
For DME and IDTFFAQ
Still have one? Our clinical team will walk you through it.
Wesper develops FDA-cleared home sleep testing medical devices. Our ecosystem brings together two wearable tests, Wesper Lab and Wesper Lite, a clinical portal, and a managed service for dropship, patient support and optional interpretation.
Wesper devices show 95%+ AHI correlation to in-lab polysomnography (PSG), with narrow limits of agreement (Sleep Medicine 2025; JCSM 2023).
Wesper Lab uses two patches on the chest and abdomen to capture direct respiratory data, including an FDA-cleared airflow signal without a nasal cannula. Wesper Lite is a PPG-based sleep test in a ring format that is easy to deploy and easy for patients to use.
No. Wesper Lab measures an FDA-cleared airflow signal from its two wearable patches, so patients sleep without a nasal cannula.
Yes. Multi-night testing comes standard with Wesper, and repeat studies stay on the same patient record for longitudinal follow-up.
Yes. Wesper is HIPAA compliant and holds SOC 2 Type 2.
Wesper home sleep tests are ordered by healthcare providers for their patients. Patients complete the sleep test at home. Wesper home sleep tests are indicated for adult use only.
Get Started
A walkthrough of the devices, the portal and how a Wesper program would run for your patients.