Technology
The Problem
Revision implant extraction is often the most time-consuming step in revision arthroplasty. Well-fixed components can require prolonged mechanical disruption (osteotomes, burrs, trephines) and sometimes invasive exposure, extending operative time and increasing risk of bone loss, fracture, debris, infects and other complications.
MicoCalo Implant Extraction Assist System (MIEAS)
How induction heating works
Why low induction frequency?
An induction coil transmits energy through a time varying electromagnetic field. When alternating current flows through the coil windings, it generates an oscillating magnetic field in the space within and around the coil. If a conductive metallic orthopedic implant is positioned within that field, electromagnetic induction occurs and circulating currents (eddy currents) are induced within the implant. Because the implant has finite electrical resistance, these induced currents dissipate energy as heat through resistive (Joule) heating. Importantly, the frequency of the applied field influences how energy distributes within the metal.
At higher frequencies, induced currents tend to concentrate near the surface of the conductor due to the skin effect, limiting penetration depth.
At lower frequencies, current penetration increases, allowing energy deposition deeper into the implant cross-section. This can promote more volumetric and uniform heating rather than surface-localized heating. Uniform energy distribution is particularly relevant in orthopedic implants, which often contain geometric transitions such as edges, corners, tapers, holes, or modular junctions.
We utilize a low frequency induction system.

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Because seeing is believing
This was one of the bench tests performed after ~3 minutes of heating from room temperature.
If video's don't work here:Hip ImplantKnee Implant
If video's don't work here:Hip ImplantKnee Implant

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Patent Progress
FDA Regulatory Progress
Micocalo filed a PCT application in 04/28/2023 We are currently pursuing this filing the EPO and USPTO
Micocalo has identified 2 predicate devices that did not require clinical trials. We are filing a q-submission to seek regulatory guidance on the testing required for a 510k application for this device.
Secondary Biofilm Application
Additionally, this system has been used to render biofilms more susceptible to antibiotics. Below is some of our initial data we obtained. We grew MRSA on metal coupons and treated them with device at much lower settings, while monitoring the temperature. These results were obtained with MIC levels of antibiotics.