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New • Surgical Series

Reinventing Microscopes
one lens at a time.

Optical performance, ergonomics and illumination designed for clinical workflows. Optional companion app available.

The Mobile Series

DP Mini

A smartphone-powered stereoscopic microscope. Compact, portable, and designed to bring 3D optical precision wherever it's needed.

01 — Overview

A microscope in your pocket.

The first system to turn a smartphone into a true stereoscopic microscope. Using an innovative optical architecture, it captures 3D images from a single mobile sensor.

  • ✓ Active stereoscopic system
  • ✓ Compact, portable design
  • ✓ AR/MR Integration
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02 — Intended Use

Built for the operating room.

The DP Mini is an active Class I medical device intended for magnified visualization of the surgical field and anatomical structures during medical and surgical procedures. It acts exclusively as a visual aid to the qualified clinician — it does not perform diagnosis, measurement, or therapy.

Dentistry & Oral Surgery
Endodontics, implantology, conservative procedures.
Neurosurgery
Microsurgical visualization of fine neural structures.
ENT
Otorhinolaryngology procedures in the ear, nose and throat.
Ophthalmology
High-resolution imaging for ocular procedures.
Plastic & Reconstructive
Fine suturing and microvascular work.
General Surgery
Visual support for procedures requiring detailed observation.
Training & Simulation
Medical education, documentation and telementoring.
Contraindications
Not for MRI environments, flammable anesthetic mixtures, or direct sterile contact. MR Non-Safe.
The Digital Surgical Series

DP Pro

A full digital surgical microscope built on a 3-axis gimbal stabilization platform. Engineered for high-precision procedures where absolute stability is non-negotiable.

01 — Overview
Coming Next

Stability, redefined.

A revolutionary digital surgical microscope that redefines stability. The optical body moves independently on a gimbal stabilization system, offering unparalleled precision. Available after the DP Mini launch.

  • ✓ 3-axis gimbal stabilization
  • ✓ Articulated extensible arm
  • ✓ AI Surgical Guidance
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02 — What's Next

Full specs reveal at launch.

The DP Pro technical datasheet is being finalized while the system completes verification testing. Specifications, certifications and pricing will be published when the device launches — right after the DP Mini reaches surgeons.

In development

3-axis gimbal stabilization

Decoupled optical body for image stability through long procedures.

In development

Articulated robotic arm

Counter-balanced reach with electromagnetic lock-in-place.

In development

AI surgical guidance

An optional, non-diagnostic visual aid layered over the live field.

In development

Med Connect Pro

Streaming, recording and telementoring built into the OR.

The Ecosystem

Dedicated Software

Explore the suite

Components & Technology

Built with the best in the industry

Apple Blackmagic Design Edmund Optics JLCPCB Cubemars Amuse Cloomtech Craftcloud
Family Driven Innovation

The Minds Behind DP Biotech

A family heritage of engineering excellence, bridging mechanics and digital intelligence.

Franco Dal Pont

Franco Dal Pont

R&D & Patent Manager

The architect of our mechanics. Franco leads 3D modeling and manages the intellectual property that drives our optical innovations.

Giorgio Dal Pont

Giorgio Dal Pont

Software & Workflow Design

Bridging the gap between user and machine. Giorgio architects the software ecosystem and defines clinical workflows.

Marco Dal Pont

Marco Dal Pont

Software & Product Design

Designing the digital experience. Marco oversees the interface design and software logic that powers the Med Connect suite.

Questions & Answers

Frequently asked

Everything procurement, clinical staff and biomed engineers usually ask us.

Yes. The DP Mini is a Class I active medical device under Regulation (EU) 2017/745 (MDR), self-certified by the manufacturer according to Art. 19 MDR. Dal Pont Medical S.r.l.s is registered in EUDAMED under SRN IT-MF-000052836. The full Technical File and EU Declaration of Conformity are available to authorities and qualified buyers on request.
The DP Mini operates exclusively in combination with an iPhone 17 Pro (or later) running iOS 26.0 or higher and the dedicated Med Connect app. The smartphone acts as the main processing unit; at least 3.0 GB of free memory and active permissions for camera, Bluetooth, NFC and local network are required. The iPhone is not included.
No. The DP Mini is classified MR Non-Safe. It contains metallic components and electronic modules that are incompatible with high-intensity magnetic fields. Use in MRI environments is an absolute contraindication, along with use in the presence of flammable anesthetic mixtures, concentrated oxygen, or nitrous oxide.
The device is supplied non-sterile and cannot be sterilized by any method (autoclave, EtO, plasma). If used in proximity to the surgical field, it must be protected with a certified single-use sterile drape. Direct contact with open wounds, mucosae or sterile tissues without a sterile barrier is not permitted.
The expected service life is 10 years from the date of manufacture, provided the use and maintenance instructions in the user manual are followed. The LED illumination module has an estimated average lifetime of ≥ 10,000 hours and is available as a replacement part.
The coaxial LED source has been evaluated under EN 62471 (photobiological safety) and classified as Risk Group 1 (Low) at the standard 30 cm operating distance. The user manual instructs operators not to stare directly into the beam, and intensity is adjustable from 0 to 100%.
Yes. The Med Connect app is developed according to Safety by Design principles and complies with GDPR (Regulation EU 2016/679). Bluetooth pairing is authenticated, data is protected by native iOS security (Face ID / passcode), and the software follows the cybersecurity requirements of MDR Annex I, 17.2 and MDCG 2019-16 guidance.
The DP Mini is intended for use by qualified healthcare professionals — surgeons, medical specialists, and trained OR technicians. Users must read the user manual thoroughly before operating the device. Use in pediatric patients is permitted under the responsibility of the qualified clinician.
Any serious incident involving the device should be reported immediately to Dal Pont Medical S.r.l.s at support@dpbiotech.com and to the competent authority of the Member State in which the user is established. Our PRRC (Person Responsible for Regulatory Compliance) is Franco Dal Pont — dalpontfranco@dpbiotech.com.

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