DEPLOYThe reference layer for physical AI

Robot model

Happy Ring

Happy Ring is a finger-worn smart ring made by Happy Health Inc of Austin, Texas, and it is recorded in the biometric form factor as the within-cohort genuinely-FDA-cleared sleep-apnea exemplar, the verified counterpoint to uncleared sleep-apnea claims elsewhere in the cohort. Its sensor stack of four LEDs, four electrodes, a three-axis accelerometer, and two temperature sensors yields heart rate, heart-rate variability, blood-oxygen saturation, skin temperature, respiratory rate, activity, and sleep staging, and the value of the device is its cleared sleep-apnea algorithm. It holds two FDA 510(k) clearances: K240236, decided October 8, 2024, for retrospective remote monitoring of physiological parameters in adults at home or in healthcare facilities, and K242224, decided June 18, 2025, a Home Sleep Test that processes ring signals for clinician-interpreted diagnosis of sleep disorders such as obstructive sleep apnea and insomnia in individuals aged twenty-two and older under the direction of a trained healthcare provider. The first clearance is best read as monitoring and the second as diagnosis-facilitating, so the genuinely-FDA-cleared framing holds while the diagnosis is clinician-mediated rather than autonomous, and the registry does not extend the claim beyond the cleared indication. Several cap-flags apply. The widely-cited figure of about ninety-seven percent agreement with gold-standard polysomnography is company-reported and has no peer-reviewed citation found, with the company's own technology page instead stating the softer claim of being ten times more accurate than a watch. Commercial availability is service-gated and thin: the ring is sold only bundled into the clinician-reviewed Happy Sleep home-sleep-test service, which is insurer-billed, rather than as a standalone retail ring with a published consumer price, and the company raised a sixty-million-dollar Series A in August 2022 led by ARCH Venture Partners with no later round surfaced, so it is an early-stage and quiet company; the maturity is recorded as commercial because the cleared service is live and billed, with the cap-flag preventing over-reading the FDA clearance as broad market presence. Finally, marketing references to brain activity or brain biometrics are flagged as marketing-forward because no EEG sensor is itemized on the spec page. The chief executive is Dustin Freckleton, MD.

Happy Ring is a biometric robot built by Happy Health.

Machine-readable surfaces

Form factor
biometric
Maturity stage
commercial
Lifecycle
active
Deployments
0
ID
2af2d126-5e1a-4636-ac6f-cc5e0f8bbe1f

Specs

notes
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
specs
Happy Ring: finger-worn smart ring. Sensors: 4 LEDs, 4 electrodes, 3-axis accelerometer, 2 temperature sensors -> heart rate, HRV, SpO2, skin temperature, respiratory rate, activity, sleep staging. Cleared sleep-apnea algorithm is the regulatory substance. Two FDA 510(k) clearances: K240236 (Oct 8 2024) = retrospective remote MONITORING of physiological parameters in adults at home or in healthcare facilities; K242224 (Jun 18 2025) = Home Sleep Test that processes ring signals for clinician-interpreted DIAGNOSIS of sleep disorders such as obstructive sleep apnea and insomnia, ages 22+, under direction of a trained healthcare provider. Company: Happy Health Inc (Austin TX); CEO Dustin Freckleton MD; $60M Series A (Aug 2022, ARCH Venture Partners), no later round surfaced. Distribution: sold ONLY bundled into the clinician-reviewed 'Happy Sleep' home-sleep-test service (insurer-billed), NOT a standalone retail ring; no published consumer price.
formFactor
biometric (biometric-primary smart ring; FDA-cleared sleep-apnea / sleep-disorder DIAGNOSIS support via clinician-reviewed home sleep test)

Supply chain

No verified supply relationships on file. Supply-chain coverage is being added across the registry; check back as the seed populates this model’s suppliers.

Suppliers appear here when verified with at least two strong sources (maker-official / IR / regulatory / standards-body / verified tier-2). Sources are append-only; corrections add new sources rather than rewrite history.

Sources (7)

  1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K242224
  2. https://aasm.org/fda-clears-happy-ring-by-happy-health/
  3. https://www.biospace.com/press-releases/happy-ring-earns-second-fda-clearance
  4. https://happysleep.com/tech
  5. https://www.finsmes.com/2022/08/happy-health-raises-60m-in-series-a-funding.html
  6. https://openloophealth.com/news/openloop-expands-into-sleep-diagnostis-with-happy-sleep
  7. https://sleepreviewmag.com/sleep-diagnostics/home-testing/home-apnea-testing/happy-ring-maker-ensodata-offer-home-sleep-testing-solution/

Common questions

What is Happy Ring?
Happy Ring is a finger-worn smart ring made by Happy Health Inc of Austin, Texas, and it is recorded in the biometric form factor as the within-cohort genuinely-FDA-cleared sleep-apnea exemplar, the verified counterpoint to uncleared sleep-apnea claims elsewhere in the cohort. Its sensor stack of four LEDs, four electrodes, a three-axis accelerometer, and two temperature sensors yields heart rate, heart-rate variability, blood-oxygen saturation, skin temperature, respiratory rate, activity, and sleep staging, and the value of the device is its cleared sleep-apnea algorithm. It holds two FDA 510(k) clearances: K240236, decided October 8, 2024, for retrospective remote monitoring of physiological parameters in adults at home or in healthcare facilities, and K242224, decided June 18, 2025, a Home Sleep Test that processes ring signals for clinician-interpreted diagnosis of sleep disorders such as obstructive sleep apnea and insomnia in individuals aged twenty-two and older under the direction of a trained healthcare provider. The first clearance is best read as monitoring and the second as diagnosis-facilitating, so the genuinely-FDA-cleared framing holds while the diagnosis is clinician-mediated rather than autonomous, and the registry does not extend the claim beyond the cleared indication. Several cap-flags apply. The widely-cited figure of about ninety-seven percent agreement with gold-standard polysomnography is company-reported and has no peer-reviewed citation found, with the company's own technology page instead stating the softer claim of being ten times more accurate than a watch. Commercial availability is service-gated and thin: the ring is sold only bundled into the clinician-reviewed Happy Sleep home-sleep-test service, which is insurer-billed, rather than as a standalone retail ring with a published consumer price, and the company raised a sixty-million-dollar Series A in August 2022 led by ARCH Venture Partners with no later round surfaced, so it is an early-stage and quiet company; the maturity is recorded as commercial because the cleared service is live and billed, with the cap-flag preventing over-reading the FDA clearance as broad market presence. Finally, marketing references to brain activity or brain biometrics are flagged as marketing-forward because no EEG sensor is itemized on the spec page. The chief executive is Dustin Freckleton, MD.
Who makes Happy Ring?
Happy Ring is made by Happy Health, based in Austin, Texas, USA.
Where is Happy Ring deployed?
No verified deployments of Happy Ring are currently on the DEPLOY registry. DEPLOY records deployments only when verified at a named site with a primary source; absence may reflect pre-deployment, research, or manufacturer-internal use.
What is Happy Ring's maturity stage?
Happy Ring is at the commercial stage on the DEPLOY maturity ladder (research, prototype, pilot, commercial, production). Commercial stage means production-grade deployments are operating at named customer sites.

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