4th State MedicalRegenerative · Technology
Medical Device Development

A connected device platform designed for the future of regenerative care.

4th State Medical is developing a next-generation medical device concept intended to integrate connected operation, consumable traceability, and clinical workflow support.

Platform status
Concept
Regulatory status
Pre-submission
Availability
TBD
Intended use
Under review
Development Focus

What we are engineering now.

The device program is focused on establishing a robust technical and regulatory foundation before any commercial release. The following priorities guide current engineering, quality, and regulatory work.

  1. 01Clinical need & concept definition
  2. 02Industrial & medical-grade design
  3. 03Quality-system planning
  4. 04Risk management & design controls
  5. 05Safety & performance testing
  6. 06Consumable compatibility analysis
  7. 07Human-factors evaluation
  8. 08Cybersecurity & data protection
  9. 09Regulatory classification & pathway
  10. 10Preclinical & clinical evidence planning
Conceptual Capabilities

What the platform is designed to enable in the future.

Connected Operation

Future device architecture designed to record session parameters, verify operating state, and support consistent use across clinical settings.

Consumable Authentication

Intended capability to verify consumable identity and compatibility before use, helping reduce mismatched or expired components.

Lot & Expiration Tracking

Planned data capture for lot numbers, expiration dates, and supply-chain traceability linked to each device-use session.

Usage Logging

Future device-use session records designed to support quality review, training feedback, and structured outcomes data collection.

Inventory Alerts

Planned automated notifications for consumable levels, expiration proximity, and replenishment needs.

Cloud Connectivity

Future secure synchronization with a cloud platform for device management, dashboard access, and data governance.

Clinical Workflow Integration

Designed to align with existing clinical processes, EMR interoperability objectives, and multi-user care-team environments.

Outcomes Data

Intended support for structured data collection to enable real-world evidence, quality reporting, and study participation.

Future AI Compatibility

Architecture planned to accommodate future analytics, protocol benchmarking, and decision-support tools developed under appropriate regulatory frameworks.

Concept Platform

4th State Fusion

A dual-handpiece concept console designed to unify device operation, consumable authentication, and session data capture within a single connected workstation. Final industrial design, materials, user interface, and feature set are subject to change through engineering iteration, testing, and regulatory review.

Placeholder notice: Final device renderings, engineering specifications, and connected-system diagrams will replace this concept as development milestones are completed.

NoticeFinal design, features, intended use, regulatory classification, and commercial availability are subject to ongoing development, verification, validation, and regulatory review. This page does not describe a cleared or available medical device.
4th State Fusion concept device — dual-handpiece console with touchscreen display
Concept Rendering
4th State Fusion — Under Development
Connected Ecosystem

How device, consumable, and data may work together.

01
Device
  • Connected operation
  • Usage logging
  • Cloud sync
02
Consumable
  • Authentication
  • Lot tracking
  • Expiration alerts
03
Data & Workflow
  • Clinical dashboard
  • Outcomes data
  • Future AI analytics
NoticeThis ecosystem diagram describes future design intent. Actual capabilities, data flows, integrations, and AI functionality will depend on technical development and regulatory authorization.
Regulatory Path

A disciplined route from concept to future authorization.

The device program is expected to follow a structured quality-system and regulatory pathway. The specific submission type, testing scope, and permitted claims for any product will be determined only after regulatory analysis based on the final intended use and technological characteristics.

NoticeDevice concepts, capabilities, and features described on this page reflect areas of active development and future intent. They do not represent cleared, approved, or commercially available medical devices, and no representation is made about diagnosis, treatment, cure, prevention, or mitigation of disease.