The Instrument.
A tri-axis Helmholtz coil array with embedded near-infrared emitters and integrated bioregulator-delivery synchronization. Three orthogonal coil pairs generate spatially structured field patterns with sub-millimeter resolution. The patient is positioned at field-center; the four-layer protocol runs across a single treatment window.
Each layer reconfigures the instrument.
Select a control layer to load the corresponding parameter envelope. Frequency and field strength can be adjusted within the envelope to match the indication. The center pulse responds in real time to the active configuration.
Reference configuration.
- Aperture
- Ø 150 mm
- Field geometry
- Tri-axis Helmholtz
- Frequency range
- 0.5 – 500 Hz
- Field strength
- 0.05 – 3.0 mT
- Optical channel
- NIR 810 / 1064 nm
- Session duration
- 45 minutes
- Control system
- AI-sequenced protocol
- Regulatory pathway
- Class II 510(k) predicate
Three coils, four emitters, one protocol.
Three orthogonal Helmholtz coil pairs generate independently controlled magnetic fields along the X, Y, and Z axes. The superposition of three independent fields produces the spatially structured gradient required for the bioelectric pattern layer — a uniform field cannot write into morphogenetic memory; only a structured one can.
Four near-infrared emitters at 45° angles around the aperture provide concurrent optical and magnetic stimulation. The peer-reviewed wound-care literature documents a supra-additive effect — combined exposure produces cellular responses that exceed the sum of either modality applied in isolation.
Onboard control sequences the four-layer protocol and synchronizes bioregulator administration to the cellular state that maximizes uptake. Each indication has a tuned envelope of frequency, field strength, NIR wavelength, and bioregulator timing — encoded as a protocol rather than configured by hand.
A predicate device pathway.
Pulsed electromagnetic field stimulators have been a Class II cleared device category since 1979, with extensive predicate history covering non-union bone, spinal fusion, osteopenia, and soft-tissue applications. The instrument described here operates within that established scientific and regulatory framework.