NOVAMATRA
NOVAMATRA / ENGINEERING RESEARCH / 2026

STERION.
Two systems.
One mission.

Experimental footwear hygiene and controlled decontamination engineering. Two parallel product architectures: CORE and INSERT.

Research and prototypingNot commercially available
Open technical archiveExplore product architectures
01 / Two development paths

CORE and INSERT

ST–CORE / CLOSED CHAMBER

STERION CORE

A closed-chamber platform designed to hold an entire shoe. Industrial design direction approved, but exact treatment geometry, interlocks and photobiological protection remain under development.

Mechanical studyV0.9 / CAD
Engineering reviewREV10
Manufacturing statusNot released
Microbial validationPending
ST–INSERT / COMPACT

STERION INSERT

Two compact inserts connected to a shared external base, with STEP/STL test geometry and an experimental mounting map.

Design revisionREV11 / P1–M0
BASE188 × 132 × 64 mm
Experimental mounting positions18 × M3
Microbial validationPending
02 / Safety and test evidence

Four functions; evidence before claims.

01 / REMOVE

Physical particle removal

Air transport and extraction testing. Surface removal is measured separately from actual filtration capture.

02 / ACTIVE

Surface treatment research

Assessment of antimicrobial processes targeting inner footwear surfaces. No demonstrated efficacy yet.

03 / VERIFY

Control, containment and testing

Interlocks, traceable measurements and independent validation before making any disinfection claim.

No sterilization, virus or fungal elimination efficacy, or safety certification has been demonstrated. UV-C for CORE requires validated containment and safety interlocks; INSERT must not emit UV-C into an open shoe.

03 / Integrated technical archive

One entry point for STERION engineering.

Master package with research reports, external studies, versioned software, experimental CAD, STEP/STL, technical analysis, and visual reference material. Both products and revision history are included.

17 source filesConsolidated technical sources
7.9 MBMaster ZIP archive
2026-11-05Archive compilation
Full technical archive / 2026-11-05

CORE + INSERT / Master Package

The ZIP is hosted on Google Drive with restricted access. Authorization from the owner may be needed.

SHA-256: 83bec2c7225a0f36a99439b164e92cc96f2d7b994639c65a4b5a5bdd033f399f
Open full technical archive
04 / Next engineering milestones

From drawings to tested hardware.

  1. G1
    Select actual parts and confirm interfaces
    Supplier datasheets, holes, gaskets, fasteners, and dimensional assembly tests.
  2. G2
    Measure pressure, flow, and particle capture
    Real hardware data for airflow, electrical power, sound, and inert particle balance.
  3. G3
    Design a contained antimicrobial process
    Treatment selection, containment, material compatibility, and appropriate safety engineering.
  4. G4
    Independent microbiological validation
    Material-specific and location-specific reduction tests in qualified laboratories.
  5. G5
    Release an actual manufacturing revision
    Only after controlled drawings, verified components, and material risks are resolved.