AIOMEGA® AIO BREATHE®: FDA CLEARED FOR PEDIATRIC & ADULT OBSTRUCTIVE SLEEP APNEA

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    • HOME
    • Clinicians
    • Patients
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    • PARTNERS & portal
    • Investors
    • About & Regulatory
    • Contact
  • HOME
  • Clinicians
  • Patients
  • Technology
  • Device
  • PARTNERS & portal
  • Investors
  • About & Regulatory
  • Contact

Investor Relations

Advancing precision intraoral medical technologies through responsible innovation.

  

 AIOMEGA® develops clinician‑directed intraoral medical devices supported by engineering rigor, regulatory compliance, and a disciplined product‑development strategy. Our focus is long‑term value creation through technology, quality, and responsible growth. 

 

Company Overview


 AIOMEGA® is a clinician‑centered medical technology company focused on advancing intraoral device therapy through engineered biomechanics, digital precision, and responsible innovation. Our development philosophy emphasizes safety, material biocompatibility, manufacturing consistency, and transparent communication with clinicians, partners, and stakeholders. 


Investment Philosophy

 

AIOMEGA® prioritizes sustainable growth grounded in engineering excellence, regulatory awareness, quality‑system discipline, clinician‑centered design, and responsible commercialization. Our long‑term value is built on:

  • Technology innovation
  • Intellectual property development
  • Clinical partnerships
  • Manufacturing consistency
  • Responsible market entry

We focus on solving unmet needs while being mindful of cost, complexity, and the realities of modern healthcare.


Intellectual Property Portfolio

 

The AIOMEGA® IP estate, assigned to Sleep Solutions of Texas, LLC, includes a broad portfolio of granted patents and pending applications covering innovations in:

  • Intraoral device geometry
  • Mandibular positioning systems
  • Digital workflows
  • Biomechanical modeling

A full list of granted and pending patents is available upon request. This summary is provided for informational purposes only and does not disclose proprietary internal logic or unpublished technologies.


Regulatory & Quality Commitment

 

AIOMEGA® follows a development approach informed by established regulatory principles and quality‑system expectations. Our processes incorporate:

  • QMSR‑aligned quality practices
  • ISO 13485‑style design controls
  • ISO 10993‑compliant material selection
  • Validated manufacturing workflows
  • Device‑level traceability
  • Structured post‑market surveillance

These references describe the concepts that guide our internal processes and are not intended to imply certification or regulatory designation.



Partnership & Collaboration


AIOMEGA® collaborates with clinicians, research groups, and technology partners to advance intraoral device innovation. We welcome discussions with strategic partners who share our commitment to responsible development, clinical clarity, and long‑term value creation. 


 

Leadership


AIOMEGA® was founded by Raghavendra V. Ghuge, MD, DABSM, FAASM, MBA, an adult and pediatric sleep physician with more than 20 years of clinical experience in sleep medicine. Dr. Ghuge combines medical training with engineering‑driven device development and business expertise from the Duke University Fuqua School of Business. His work spans clinical care, invention, intellectual‑property development, and the creation of clinician‑directed digital workflows that emphasize safety, clarity, and responsible innovation.



Investor Inquiries

For investor or strategic partnership inquiries, please contact: 

Email: info@aiomd.com


Please include your name, organization, contact information, and area of interest.



© 2026 AIOMEGA®. All rights reserved. AIOMEGA® is a registered trademark of Sleep Solutions of Texas, LLC. This page is for informational purposes only and does not constitute an offer to sell or a solicitation of an offer to buy securities.

Copyright © 2026  AIOMEGA®  LLC - All Rights Reserved.


  AIOMEGA® — Advanced Intraoral Medical Devices

Information on this site does not replace professional medical advice.

Use of all devices must follow FDA-cleared labeling and clinician supervision.

Prescription-only medical devices. See FDA-cleared labeling for full safety information. 

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AIOMEGA® SLEEP 2026 - Booth #968

  We’re excited to welcome you to SLEEP 2026 in Baltimore. Visit Booth #968 to meet the AIOMEGA® team and preview our latest clinical innovations.

Join us for three national poster presentations on June 15–16, featuring new research in:

  • Adult OSA therapy
  • Pediatric PDS outcomes
  • Next‑generation digital workflows

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