SPUTA VACUUMER®: A Paradigm Shift in Airway Clearance

SPUTA VACUUMER®

Reversing the Concept: “Don’t Chase Sputum. Make it Come to You.”

Traditional suction is painful and risky because it requires inserting a tube deep into the lungs. SPUTA VACUUMER® changes everything. By applying a unique “Vacuuming” theory, we move the sputum to the catheter, not the other way around. This enables safe, simple, and low-invasive suction for any practitioner.

Estimated Business Value

JPY 1.9 Billion+

Target Market

Global “Blue Ocean” in Airway Management

Disclaimer: This valuation is a conceptual estimate by an AI and is not a substitute for an official market transaction appraisal. It should be used for reference purposes only.

The Core Innovation

The Challenge: A Reality of Pain and Risk

Traditional suction procedures inflict severe distress (gagging, pain) and complication risks (airway damage, hypoxemia) on patients. Existing alternatives like mechanical insufflation-exsufflation (MI-E) face significant hurdles: High Cost and Complex Operation.

STONY’s Solution: The “Vacuuming” Paradigm Shift

We developed a universal connector that converts standard suction pressure into a therapeutic “Vacuuming” force.

Universal: Compatible with standard endotracheal tubes and LMAs.

Low Cost: Uses existing suction pumps.

High Safety: No need for deep insertion.

the caring hands

For Patients: Liberation from Pain

Transforms a “torturous procedure” into “gentle care.” Dramatically improves QOL by reducing coughing fits and mucosal damage.

the burden lifted

For Caregivers: Skill-Free Safety

Standardizes the technique. Enables even less-experienced staff or family members to perform safe suctioning, reducing the burden of care and risk of human error.

the expanding market

For Business: Recurring Revenue

Establishes a powerful Recurring Revenue Model based on high-volume disposables. A massive, untapped market awaits in home care, elderly care, and ICUs.

Commercial Readiness & IP Protection

1. Development Stage: Ready to Launch

  • Regulatory Approved: Japan PMDA Class I (General Medical Device).
  • Mass Production: Established at our “Mother Factory” (Tochigi Seiko Co., Ltd.) in Japan. High-quality injection molding lines are operational.

2. An Ironclad IP Portfolio

This system is protected not by a single patent, but by a multi-layered web of rights, making imitation extremely difficult.

  • Foundational Patent: The core “Vacuuming” mechanism.
  • System Patent: Enabling safe clinical application.
  • Global Coverage: Patents granted/pending in Japan, USA, Europe, China, and India.

Partnership Opportunity

We are seeking Global Licensing Partners to expand this “Standard of Care” worldwide.

  • India/Asia: Perfect for high-volume, cost-sensitive markets.
  • US/EU: Ideal for high-value home care and infection control markets.