Full-Time
FDA-approved wearable tremor therapy device
$140k - $165k/yr
H1B Sponsorship Available
San Mateo, CA, USA
Hybrid
Three days on-site per week required; local candidates only.
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Cala Health develops the Cala kIQ System, a physician-prescribed wearable that treats hand tremors from essential tremor and Parkinson’s disease using TAPS therapy. TAPS is a non-invasive electrical stimulation of skin nerves delivered via the wearable during roughly 40-minute sessions to reduce tremors. The device collects patient data to help patients and doctors monitor progress and tailor care, blending non-drug therapy with existing medications. It differentiates itself by FDA-approved, physician-prescribed, non-invasive, data-driven therapy that complements medical treatment, with the goal of improving daily tremor management and supporting measurable clinical outcomes.
Company Size
51-200
Company Stage
Growth Equity (Venture Capital)
Total Funding
$298.3M
Headquarters
San Mateo, California
Founded
2014
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Hybrid Work Options
Cala Health wins 2026 MedTech Breakthrough award for Best New Neurology Technology Solution. Cala Health | 14 May 2026 SAN MATEO, Calif., May 8, 2026 /PRNewswire/ - Cala(R), the bioelectronic medicine leader, announced today the Cala kIQ(R) System has been named "Best New Neurology Technology Solution" as part of the 2026 MedTech Breakthrough Awards. The awards honor excellence and recognize innovation, hard work, and success in various health and medical technology categories. This year's program attracted more than 5,000 nominations from around the globe. Cala Health won the award in recognition of its groundbreaking neurology technology platform, which is transforming how patients struggling with essential tremor (ET) access and receive care. The company is part of an elite group of 2026 winners that includes Noom, Boston Scientific, Teladoc, Medtronic, DocGo, Zimmer Biomet, CVS Health, Lyra Health, Elsevier, Medidata, IQVIA, Thermo Fisher Scientific, PointClickCare, Canon Medical Systems, and Alcon/Novartis among others. "Being named the Best New Neurology Technology Solution by the MedTech Breakthrough Awards is a meaningful validation of the work our entire team has poured into making Cala TAPS(R) Therapy a reality for patients living with essential tremor," said Deanna Harshbarger, CEO of Cala Health. "For too long, people with ET have had limited options that fit into their daily lives. We set out to change that with a non-invasive, wearable therapy they can use at home. This recognition reflects not just our technology, but our commitment to expanding access. We're proud of how far we've come, and even more energized about what's ahead." The Cala kIQ system delivers TAPS Therapy through a noninvasive wrist-worn wearable neuromodulation device, which is physician-prescribed and aids in the temporary relief of hand tremors in adults with ET. The disease affects over 7 million Americans, causing uncontrollable hand and arm shaking that disrupts daily activities, and pre-existing treatment options are often insufficient or require invasive surgical options. The Cala kIQ System bridges this treatment gap and eases symptoms in the treated hand following stimulation. For more on how Cala Health is transforming neurology care, visit www.calahealth.com. About Cala*(R) Cala Health(R)* is a bioelectronic medicine company transforming the standard of care for chronic disease. The company's wearable neuromodulation therapies merge innovations in neuroscience and technology to deliver individualized peripheral nerve stimulation, and its direct-to-home digital durable medical equipment (DME) platform is reshaping the delivery of prescription therapies. The Cala kIQ(R) System is the only FDA-cleared wearable device that delivers effective therapy for action hand tremor in people with essential tremor and Parkinson's disease. The Cala kIQ device is indicated to aid in the temporary relief of hand tremors in the treated hand following stimulation in adults with essential tremor. The Cala kIQ device is indicated to aid in the temporary relief of postural and kinetic hand tremor symptoms that impact some activities of daily living in the treated hand following stimulation in adults with Parkinson's disease. The Cala kIQ device delivers TAPS(TM) therapy, which provides transcutaneous afferent patterned stimulation. Caution: Federal law restricts this device to sale by or on the order of a physician. Prior to use, refer to the product labeling for complete product instructions for use, contraindications, warnings, and precautions at https://calahealth.com. SOURCE Cala Health
Cala health wins 2026 MedTech Breakthrough award for best New Neurology Technology Solution. SAN MATEO, Calif., May 8, 2026 /PRNewswire/ - Cala(R), the bioelectronic medicine leader, announced today the Cala kIQ(R) System has been named "Best New Neurology Technology Solution" as part of the 2026 MedTech Breakthrough Awards. The awards honor excellence and recognize innovation, hard work, and success in various health and medical technology categories.
Trinity Capital has committed $50 million in growth capital to Cala Health, a bioelectronic medicine company developing wearable therapies for tremors. The funding will support commercial expansion of Cala's FDA-cleared kIQ System. The wearable device helps patients manage hand tremors caused by essential tremor and Parkinson's disease. Worn on the wrist, it measures individual tremor patterns and delivers personalised nerve stimulation through noninvasive electrical stimulation. The therapy is prescribed by physicians for at-home use, enabling patients to perform everyday activities like reading, writing and eating. Trinity Capital, a Phoenix-based alternative asset manager, has deployed over $5.5 billion across more than 463 investments since 2008. The partnership aims to optimise Cala's capital structure whilst accelerating product innovation and commercial growth.
In psychedelics and neuroscience... Cala Health announced FDA clearance of its next-generation Cala kIQ Plus wearable, a new upgrade to its existing neurostimulation platform for essential tremor and Parkinson's disease. The device builds on its TAPS (transcutaneous afferent patterned stimulation) technology, adding new therapy modes and adaptive calibration designed to improve tremor control and personalize treatment delivery. The updated system allows patients greater control over when and how therapy is delivered, while early clinical data suggest improved response rates and broader efficacy, including bilateral tremor improvement. Check it out: https://www.prnewswire.com/news-releases/cala-announces-fda-clearance-of-its-next-generation-taps-therapy-wearable-device-for-essential-tremor-and-parkinsons-disease-302742780.html. Compass Pathways announced a U.S. grant program to fund the development of training programs for healthcare providers ahead of a potential commercial launch of its psilocybin-based therapy, COMP360. COMP360, a synthetic psilocybin therapy for treatment-resistant depression. The company is now positioning for a potential filing and approval timeline. The grant program is designed to ensure providers are trained, operationally ready, and aligned with regulatory standards, which is critical for a therapy that requires supervised administration rather than traditional prescribing. Here's more: https://ir.compasspathways.com/News-Events-/news/news-details/2026/Compass-Pathways-Announces-U-S-Grant-Program-for-the-Creation-of-Post-Approval-COMP360-Provider-Training/default.aspx. Roche received CE marking in Europe for its Elecsys Neurofilament Light Chain (NfL) blood test, allowing its commercial use across the region. The test measures levels of a protein released when nerve cells are damaged, offering a direct, blood-based signal of neurological activity instead of relying solely on periodic MRIs or symptom tracking. NfL is also not disease-specific, with elevated levels seen across multiple neurodegenerative conditions, including Alzheimer's and traumatic brain injury. That positions the test as part of a broader move toward blood-based biomarkers as a core tool in neurology, rather than a single-use diagnostic. Check it out: https://jlsfund.substack.com/p/a-simple-blood-draw-could-replace Did you know? Did you know that earlier attention deficit-hyperactivity disorder (ADHD) diagnosis could be linked to a lower probability of school dropout? A recent study published in JAMA Psychiatry looked at when people are first diagnosed with ADHD and how that timing affects their long-term outcomes. Researchers found that individuals diagnosed earlier were more likely to perform better in school, continue their education, and avoid dropping out compared to those diagnosed later in adolescence. Certainly, it makes sense that early diagnosis could shape someone's progress through school and into adulthood. After all, if the condition is identified earlier, there's more time to receive support. That being said, this particular study offers real data to support that thesis. It tracked over 500,000 individuals and found that those diagnosed earlier (typically in childhood) had better grades, were more likely to pursue academic paths, and were less likely to drop out of school compared to those diagnosed later in adolescence. The takeaway is pretty straightforward. ADHD doesn't suddenly appear in high school; it's usually there earlier. But if it's not identified, students miss out on support during the years when it matters most. By the time a diagnosis happens later (often around ages 14 to 16), academic struggles may already be entrenched, and the data show dropout risk can rise significantly, in some cases approaching 30%.
Cala Health has received FDA clearance for the Cala kIQ Plus, its next-generation wearable neurostimulation device for treating action hand tremor in essential tremor and Parkinson's disease. The device uses TAPS (transcutaneous afferent patterned stimulation) technology with new therapy modes and adaptive calibration designed to optimise tremor relief. The bioelectronic medicine company will present clinical data showing improved efficacy at the American Academy of Neurology conference in Chicago on 20 April. The study demonstrates increased responder rates and bilateral tremor improvement in essential tremor patients. The Cala kIQ System is the only FDA-cleared wearable device for action hand tremor treatment. It is available through the Veterans Affairs Health System at no cost to eligible beneficiaries and has Medicare coverage for those meeting Local Coverage Criteria.