Airiant Development

Development

From clinical observation to engineering validation, each milestone reduces technical uncertainty while advancing the airway securement platform toward commercialization.

Engineering Through Iteration

Every prototype informed the next engineering decision.

1

Concept

Clinical observations identified opportunities for a different airway securement approach.

2

Engineering

Prototype iterations refined geometry, securement, retention, and clinical workflow integration.

3

Manufacturability

Design-for-manufacturing review informed materials, tolerances, part architecture, and tooling strategy.

4

Clinical Refinement

Simulated clinical use and workflow feedback guided continued design refinement.

5

Current Validation Prototype

The current prototype supports bench and simulated clinical validation before production tooling.

Every Milestone Reduces Risk

Commercial readiness is built by systematically resolving technical uncertainty before advancing to the next stage.

01

Patent

Core platform architecture supported by a U.S. utility patent filing and international PCT application.

02

Engineering

Multiple prototype revisions informed by clinical and engineering feedback.

03

Manufacturing

Manufacturing feedback incorporated into geometry, materials, and part strategy.

04

Validation

Current prototype undergoing bench and simulated clinical testing.

05

Commercialization

Building the foundation for pilot manufacturing and future clinical adoption.

Manufacturing

Manufacturing Readiness

Manufacturing planning progresses alongside engineering to reduce risk before production tooling.

DFM

Manufacturing feedback has informed geometry, tolerances, and part architecture.

Materials

Rigid substrate and elastomer overmold strategies are being evaluated for manufacturability.

Prototype Strategy

PolyJet prototypes reduce uncertainty before injection-mold investment.

Tooling

Prototype tooling quotations support production and capital planning.

Validation

Validation Strategy

Validation progresses from controlled testing to simulated clinical use before broader adoption.

Bench Testing

Quantify securement performance, migration, and retention under controlled conditions.

Simulated Clinical Use

Evaluate device performance in EMS, transport, and acute-care scenarios.

Workflow Validation

Assess usability, workflow integration, caregiver access, and device application.

Design Refinement

Translate findings into engineering improvements before production tooling.

Current Stage

Development Status

Patent Strategy

U.S. utility patent filing and international PCT application completed.

Core Engineering

Multiple engineering and prototype cycles completed.

Validation

Current validation prototype undergoing bench and simulated testing.

Manufacturing Planning

Materials, tooling, and supplier strategy remain under continued evaluation.

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