---
title: "Back to the Future: From Telesurgery to Translational Tools"
description: Exploring the advancements in telesurgery and fluorescence-guided surgery, and how QUEL Imaging accelerates clinical translation with innovative tools and solutions.
image: https://blog.quelimaging.com/hubfs/Phantoms-2016.jpg
---

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### View of Field

 Jun 27, 2025 6:05:27 AM

# Back to the Future: From Telesurgery to Translational Tools

![Picture of Ethan LaRochelle](https://app.hubspot.com/settings/avatar/925081a77283a399dbd145b49b251212) [Ethan LaRochelle](https://blog.quelimaging.com/author/ethan)

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After a week at the [Hamlyn Symposium on Medical Robotics](https://www.hamlynsymposium.org/programme-2025/), I’ve been reflecting on this year’s theme: “Back to the Future: Telesurgery in 2025.”

The first telesurgery took place on September 7, 2001, between New York and Strasbourg, France — using a robotic system that would later evolve under Intuitive Surgical. For over two decades, telesurgery remained more concept than reality.

*Until this month.*

In June 2025, the first FDA-approved telesurgery was successfully performed between Florida and Luanda, Angola. The tech has matured — and so have the use cases. I’ll admit I arrived a skeptic: surgeons are already overloaded, and remote cases add new complexity. But after this week at Imperial College, I see the future more clearly. Telesurgery’s near-term value is especially strong for training, supervision, and specialist support in regions where care gaps persist.

## Fluorescence-Guided Surgery Is on the Same Curve

The trajectory feels familiar. When I entered university in 2005, fluorescence-guided surgery had just received its first FDA clearance. Since 2021, new agents have been approved, and imaging systems are evolving across form factors — from handhelds to robotic platforms.

At [QUEL Imaging](https://www.quelimaging.com/about), we’re focused on accelerating this clinical translation. We *<3* fluorescence, but *<3* speeding up its adoption even more.

| ![Phantoms-2016](https://blog.quelimaging.com/hs-fs/hubfs/Phantoms-2016.jpg?width=702&height=988&name=Phantoms-2016.jpg) |
| --- |
| ***2016 - 6-months into my PhD.*** ✔️Gloves. ✔️Lab coat, ✔️safety glasses, ✔️Pipet, ✔️Huge graduated cylinder, ✔️Glass beaker,✔️(labeled and covered) Falcon tubes, ✔️Print-out of Python code for weights and volumes, ✔️IV bag of Intralipid, ✔️Selfie to proof  |

## A Phantom Flashback and a 3-Minute Fix

At the begining of my PhD (coming from working in software development and telecom industry for the previous 5 years), I was tasked with testing a fluorescence imaging system. The instruction: “Make a serial dilution phantom.”  
I Googled every term:

- **Phantoms**: Tissue stand-ins
- **PpIX**: Fluorophore (powder I need to mix in liquid) used for tumor detection
- **Intralipid**: Light-scattering fat emulsion, *in an IV bag*
- **Bovine** and **Porcine** blood: Why not just say cow or pig? (And, kind of gross. Also, this is available in a catalog? 🤯)
- **Pipetting**: Let’s just say my technique was… not ideal

I wrote Python scripts to calculate the dilution volumes, suited up in (too-much) PPE, and spent hours mixing and imaging. It was not fun. It was not fast. I repeated it (begrudgingly) throughout grad school.

*Back to the Future*

Today, QUEL Imaging manufactures solid [Concentration Targets](https://shop.quelimaging.com/product-category/active/characterization/concentration/) that replicate [common clinical fluorophores](https://shop.quelimaging.com/Fluorescence-targets/) like ICG, pafolacianine, IRDye 800CW, SGM-101, and Cy5.5 — with consistent optical properties and no mess.

Last week, we asked Edwin, our optical engineer, to use a concentration target to simulate a serial dilution on one of our systems.

*⏱ Total time: under 3 minutes — from measurement to data!*  
*<3 Fluorescence. <3 Speed. <3 Not cleaning expired (chunky) phantoms out of the fridge.*  
 

Our biggest competition is still the *status quo*. Anyone can build a phantom — and they should, *once*. But in industry or clinical R&D, your time is better spent solving the bigger problems.

📹 Check out the YouTube Short to see the proof:

And if you’re ready to move faster and get out of serial dilutions, we’d love to help! Please [contact us](https://shop.quelimaging.com/resources/#contact)

[standardization](https://blog.quelimaging.com/tag/standardization), [use-guide](https://blog.quelimaging.com/tag/use-guide), [fluorescencefriday](https://blog.quelimaging.com/tag/fluorescencefriday)

## Related posts

[![Animation showing Gaussian Splat of the Prototype FluoFlow Colon Phantom](https://blog.quelimaging.com/hs-fs/hubfs/QUEL_FluoFlowColon.gif?height=200&name=QUEL_FluoFlowColon.gif)](https://blog.quelimaging.com/3dgs-opsiclear-quel)

[concepts](https://blog.quelimaging.com/tag/concepts), [fluorescencefriday](https://blog.quelimaging.com/tag/fluorescencefriday), [clinical translation](https://blog.quelimaging.com/tag/clinical-translation)

## [3D Gaussian Splatting and Future Digital Twins](https://blog.quelimaging.com/3dgs-opsiclear-quel)

![Picture of Ethan LaRochelle](https://app.hubspot.com/settings/avatar/925081a77283a399dbd145b49b251212) [Ethan LaRochelle](https://blog.quelimaging.com/author/ethan) 

 Nov 14, 2025 10:45:00 AM

This week, we shared a five-day series of 3D Gaussian splats created in collaboration with...

[Read more](https://blog.quelimaging.com/3dgs-opsiclear-quel)

[![Illustration of a general spectrophotometry configured with two integrating spheres. Most commercial spectrophotometers only contain one integrating sphere. ](https://blog.quelimaging.com/hs-fs/hubfs/undefined-Oct-13-2025-06-50-47-0324-PM.png?height=200&name=undefined-Oct-13-2025-06-50-47-0324-PM.png)](https://blog.quelimaging.com/spectrophotometry-overview)

[concepts](https://blog.quelimaging.com/tag/concepts), [optical properties](https://blog.quelimaging.com/tag/optical-properties), [tissue optics](https://blog.quelimaging.com/tag/tissue-optics), [optiblox](https://blog.quelimaging.com/tag/optiblox)

## [Full-Spectrum Optical Measurements in Tissue and Phantoms](https://blog.quelimaging.com/spectrophotometry-overview)

![Picture of The QUEL Team](https://blog.quelimaging.com/hs-fs/hubfs/QUEL_Q.png?width=50&name=QUEL_Q.png) [The QUEL Team](https://blog.quelimaging.com/author/quel) 

 Oct 15, 2025 7:30:00 AM

If you're building an optical medical device (e.g., pulse oximeters, surgical guidance tools,...

[Read more](https://blog.quelimaging.com/spectrophotometry-overview)

[![Illustration of how green and red light will scatter and absorb differently in tissue. ](https://blog.quelimaging.com/hs-fs/hubfs/undefined-Oct-13-2025-05-56-25-7121-PM.png?height=200&name=undefined-Oct-13-2025-05-56-25-7121-PM.png)](https://blog.quelimaging.com/light-tissue-interaction-overview)

[concepts](https://blog.quelimaging.com/tag/concepts), [optical properties](https://blog.quelimaging.com/tag/optical-properties), [tissue optics](https://blog.quelimaging.com/tag/tissue-optics), [optiblox](https://blog.quelimaging.com/tag/optiblox)

## [Light-Tissue Interactions in Optical Medical Devices](https://blog.quelimaging.com/light-tissue-interaction-overview)

![Picture of The QUEL Team](https://blog.quelimaging.com/hs-fs/hubfs/QUEL_Q.png?width=50&name=QUEL_Q.png) [The QUEL Team](https://blog.quelimaging.com/author/quel) 

 Oct 13, 2025 3:12:06 PM

When you're developing medical imaging systems, one of the biggest challenges is understanding how...

[Read more](https://blog.quelimaging.com/light-tissue-interaction-overview)

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