License
Split by field or by territory.
Veripuremedi develops RF microneedling, pen needle, needle and cannula, and injector technology, and licenses it out. We don’t manufacture or sell devices — so we’re never competing with the company that does.
Aesthetic results have improved for a decade. Pain hasn’t. When a patient doesn’t come back, it usually isn’t because the treatment failed. It’s because it hurt.
There have been two ways to fix that: more anesthetic, or less energy. One slows recovery. The other costs you the result. Neither is a trade a practitioner wants to make.
So we work on something else: how the needle enters, and how the energy is delivered. Every invention here started as a problem the founder ran into in his own practice.
These are the subjects. The structures and the claims aren’t here yet — “Where it stands,” below, explains why.
Radio-frequency energy delivered into the skin through fine needles. Three lines of work: an electrode structure that departs from the ones in use today, the control that structure needs, and the processes that make it manufacturable at scale. The thickest part of the portfolio.
The needle and cartridge that load into a pen-type injector, aimed at the dose that stays behind after injection. The more a vial costs, the more that residue is money thrown away.
A new structure for the needle and cannula themselves. This is the part that actually meets tissue, where a small change in shape changes how it goes in.
The device injects, not the hand. Past holding a steady rate, this covers the algorithm that shapes delivery so that it hurts less.
Two applications covering topical formulations themselves, not a device.
Korean applications publish 18 months after filing (Patent Act, Art. 64). Our earliest filing is March 2026, so the first publication lands in the second half of 2027, and the last of the 27 by the end of that year.
That’s the only reason this page stops at subjects. Nothing is being held back — until publication, these simply aren’t public documents. Sign an NDA and you get the specifications and drawings as filed.
Foreign filings are under review on the PCT route. We don’t announce dates for filings we haven’t made.
Veripuremedi doesn’t manufacture or sell devices. The technology goes to the company best positioned to build it — which means we’re never across the table from our own licensee.
Split by field or by territory.
Single application or full series.
From prototype onward, when that works better for both sides.
Tell us which of the five lines you’re after. We send a technical overview of everything that can be disclosed.
Once an NDA is in place, you get the specifications and drawings for those applications.
License, assignment, or joint development — we settle the structure and the terms together.
Technology inquiries go straight to the founder.