FDA-Cleared Home Sleep Testing

Personalized sleep testing. Personalized care.

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.

  • FDA-Cleared
  • TIME Best Inventions 2026
  • SOC 2 Type 2 and HIPAA
Patient wearing two Wesper Lab sensor patches on the chest and abdomen
95%+

AHI correlation to in-lab PSG

Illustrative raw airflow, effort and SpO2 signals around an obstructive apnea, with the hypoxic burden area shaded

Featured In

Forbes, The Wall Street Journal, AARP, JCSM, AASM, Cornell Tech and other publications

The Access Gap

Most people with sleep apnea haven't been diagnosed yet.

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

Match the right test to the right patient.

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.

Two Wesper Lab wearable sensor patches

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
Wesper Lite sensor worn on a fingertip

Wesper Lite

Light. Compact. High clinical confidence.

  • PPG
  • Flow
  • SpO2
  • Heart rate
  • Respiratory rate
  • Sleep staging

95%+AHI correlation to PSG

Wesper Lite

Indicated for adult use only.

How It Works

Full service, end to end.

You order the test and make the clinical decisions. Wesper handles shipping, patient support and scoring, and results come back to your team.

  1. Order

    One click from the Wesper portal or your EMR.

  2. Dropship

    Devices go straight to the patient's door, with return shipping included.

  3. Guide

    Automated reminders, prep and check-ins, backed by 24/7 patient support.

  4. Test

    Multi-night testing comes standard with every Wesper study.

  5. Score and report

    Automatic scoring with full access to raw data for clinician review. Optional access to board-certified sleep physicians in all 50 states.

  6. Follow up

    Re-test over time on the same patient record to see whether treatment is working.

Evidence

What the data shows.

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

Illustrative multi-channel signal review with scored events
Illustrative desaturation event with area under baseline

The Wesper Portal

A portal built for clinicians.

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.

  • High fidelity automatic scoring for clinician review
  • Full access to raw data
  • Multi-night and longitudinal views across 45+ trends
  • Custom, clinic-branded reports
  • EMR-integrated ordering and results
A patient receiving a Wesper test kit at home

99%+patient success rate

For Patients

A sleep test patients can set up at home.

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.

FAQ

Questions clinicians ask us first.

Still have one? Our clinical team will walk you through it.

What is Wesper?

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.

How does Wesper compare with in-lab polysomnography?

Wesper devices show 95%+ AHI correlation to in-lab polysomnography (PSG), with narrow limits of agreement (Sleep Medicine 2025; JCSM 2023).

What is the difference between Wesper Lab and Wesper Lite?

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.

Does Wesper Lab need a nasal cannula?

No. Wesper Lab measures an FDA-cleared airflow signal from its two wearable patches, so patients sleep without a nasal cannula.

Can patients test for more than one night?

Yes. Multi-night testing comes standard with Wesper, and repeat studies stay on the same patient record for longitudinal follow-up.

Is Wesper secure and HIPAA compliant?

Yes. Wesper is HIPAA compliant and holds SOC 2 Type 2.

Who can use Wesper home sleep tests?

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

See Wesper in your workflow.

A walkthrough of the devices, the portal and how a Wesper program would run for your patients.