Dermalyser

by AI Medical Technology  · Based in Sweden → — Safer skin cancer diagnosis in seconds
Dermatology Family Medicine Oncology

Contact for details
Regulatory Status Disclosed

Overview

Dermalyser is an AI-powered decision support app designed for medical professionals to obtain a second opinion on skin lesions. It is clinically validated for accurate assessments, boasting a 96% accuracy (AUC) in evaluating skin lesions. The tool is a CE-marked medical device, compliant with EU MDR 2017/745, signifying its adherence to European medical device regulations.

The app aims to facilitate faster diagnoses, reduce unnecessary procedures, and provide greater peace of mind in clinical decisions. It functions by analyzing a dermatoscopic image captured with a smartphone, delivering AI-driven decision support in seconds. Dermalyser demonstrates 95% sensitivity and 85% specificity in melanoma detection, along with a 99.5% Negative Predictive Value (NPV) when ruling out malignancy for benign lesions.

Developed in collaboration with dermatologists and primary care physicians, Dermalyser supports a range of medical professionals including Primary Care Physicians, Dermatologists, and General Practitioners. It is designed to be an assistant, not a replacement, ensuring that the final diagnosis always remains with the healthcare professional.

The use of Dermalyser can lead to significant operational benefits, including potential 56% cost savings and a 79% reduction in unnecessary referrals, by enabling more accurate assessments and reducing overtreatment.

Reviewed by Pouyan Golshani, MD — Interventional Radiologist

Key Features

  • AI-powered decision support for skin lesions
  • 96% accuracy (AUC) in assessing skin lesions
  • CE-marked medical device (EU MDR 2017/745, Class IIa)
  • 95% sensitivity and 85% specificity in melanoma detection
  • 99.5% Negative Predictive Value (NPV) for benign lesions
  • 5-second analysis time
  • Smartphone-based dermatoscopic image analysis
  • Reduces unnecessary referrals (79% fewer)
  • Potential for 56% cost savings
  • Validated for Fitzpatrick skin types Iu2013IV

Use Cases

  • Providing a second opinion on suspected skin melanomas
  • Supporting primary care physicians and general practitioners in skin cancer diagnosis
  • Assisting dermatologists with rapid, AI-driven analysis
  • Reducing unnecessary referrals to dermatology specialists
  • Improving diagnostic accuracy and confidence at the point of care
  • Streamlining clinical workflow for skin lesion examination

What Physicians Need to Know

Key Capabilities
AI-driven decision support for analyzing dermoscopic images of suspected melanomas, providing rapid analysis (within seconds) via a smartphone app integrated with a compatible dermatoscope.
Clinical Utility
Aids licensed healthcare professionals (GPs, dermatologists) in early melanoma detection, reducing unnecessary referrals and excisions, improving patient flow, and potentially cutting clinical costs by up to 56%. It acts as a decision-support tool, with the final diagnosis remaining with the clinician.
Integration Options
Primarily a smartphone application (iOS compatible) that works with most dermatoscopes. An AI engine, DermAIM, is available via secure APIs for integration into broader healthcare platforms.
Compliance Status
CE-marked under MDR (EU) 2017/745 as a Class IIa medical device software and is GDPR compliant. A US launch is anticipated in 2027, pending FDA 510(k) clearance.
Pricing Model
Requires a license, which clinics can obtain by contacting AI Medical Technology. Specific pricing details are not publicly disclosed.
User Experience
Designed to be intuitive, fast, and user-friendly, involving three simple steps: starting the app, taking a photo with a dermatoscope, and receiving immediate analysis. It offers multilingual support (English and Swedish).
Support Quality
AI Medical Technology provides digital training, manuals, customer support with defined service levels, and onboarding assistance including installation and staff training.
Implementation Complexity
Requires a clinic license, a smartphone with the app, a compatible dermatoscope, and trained healthcare staff. Onboarding support is provided to facilitate smooth integration into clinical practice.
Evidence Base
Clinically validated through prospective multicenter trials (e.g., AI-DSMM study, NCT05172232) published in peer-reviewed journals like the British Journal of Dermatology. It achieved an AUROC of 0.960, with 95.2% sensitivity and 84.5% specificity for melanoma, and 100% sensitivity and 92.6% specificity for invasive melanomas, outperforming expert dermatologists and general practitioners in studies. The AI model was trained on over 100,000 skin lesion images.
Physician Tip

Dermalyser serves as a powerful decision-support tool, particularly valuable in primary care for initial melanoma screening and guiding referral decisions, and for dermatologists seeking a rapid second opinion. Remember, it's an assistant, not a replacement for your clinical judgment; the final diagnosis is always yours. Be mindful of its validated scope: it's intended for suspected melanomas on Fitzpatrick skin types I-IV and has specific contraindications (e.g., not for patients under 18, ulcerated lesions, or lesions outside 2mm-2cm). Leveraging this tool can enhance diagnostic confidence, streamline patient pathways, and contribute to significant cost savings by reducing unnecessary procedures.

Dermalyser primarily integrates as a smartphone application, requiring a compatible dermatoscope to capture images. For healthcare systems looking for deeper integration, the DermAIM AI engine is available via secure APIs, allowing vendors to embed its clinically validated skin lesion risk assessment capabilities directly into their existing platforms.

Details

Category Dermatology AI, Oncology AI
Pricing Contact for details
DeploymentCloud-based
Compliance
BAA Available No AI-estimated
HIPAA Compliant No AI-estimated
FDA Status No AI-estimated

Dermalyser is CE-marked under MDR (EU) 2017/745 as a Class IIa medical device software, enabling its commercial use across Europe. A US launch is anticipated in 2027 pending FDA 510(k) clearance.

Integrations
EHR Not specified
Specialties Dermatology, Family Medicine, Oncology

What the Web Says

Dermalyser is an AI-powered medical device software designed to assist healthcare professionals in the assessment of skin lesions, specifically for melanoma risk evaluation. It analyzes dermatoscopic images captured via a compatible dermatoscope attached to an iPhone, providing real-time, AI-driven assessments. Clinical studies have shown Dermalyser to have high diagnostic accuracy, often outperforming expert dermatologists and general practitioners in detecting melanoma.

Overall: Positive

Strengths

  • Clinically validated performance with high accuracy (AUC score of 0.96), surpassing expert dermatologists (0.85) and general practitioners (0.70).
  • Provides decision support in seconds, offering instant AI-powered assessments.
  • Improves cost efficiency by helping reduce unnecessary skin excisions and streamlining clinical workflows.
  • High sensitivity (95.2%) and specificity (84.5%) in detecting melanoma, with even higher rates for invasive melanomas (100% sensitivity and 92.6% specificity).
  • Designed for healthcare professionals, developed with quality-controlled dermatoscopic images and patient data.
  • High negative predictive value (99.5%), providing confidence in ruling out malignancy when a lesion is assessed as benign.

Limitations

  • Intended only for suspected melanomas and should not be used on certain types of lesions (ulcerated, very large, on mucous membranes, under nails, on palms/soles, near eyes, or previously biopsied).
  • Currently available only for iPhone.
  • Limited information available from independent tech reviewers, G2, or Capterra.
  • Some general Reddit discussions about AI in dermatology express concerns about potential for misdiagnosis if not used responsibly, or patients delaying care by relying solely on AI tools.

Based on reviews from: App Store (Apple), PR Newswire, AI Medical Technology official website, Canada Newswire, British Journal of Dermatology (via AI Support Tool Demonstrates Detection Utility for Melanoma at Primary Care Practices), Reddit

Last updated: 2026-07-31

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Press & Coverage

Cision News
Dermalyser Receives CE Mark In Europe, Paving Way to Market for World's Best Melanoma Diagnostic Decision Support Tool
AI Medical Technology has received European CE mark approval for Dermalyser, its smartphone-based diagnosis decision support tool for melanoma detection. The company plans to commence full commercial operations in Europe and aims for a US launch in 2027.
2025-05
Drug and Device World
AI-powered melanoma app Dermalyser scores EU's CE mark
Dermalyser, an AI-powered smartphone application for melanoma detection, has received CE mark approval for use across the European Union. Clinical studies show the tool significantly outperforms even experienced dermatologists in identifying melanoma.
2025-05
Dermatology Times
Dermalyser Secures CE Mark in Europe for AI-Powered Melanoma Detection Tool
AI Medical Technology announced CE mark certification for Dermalyser, an AI-driven diagnostic decision support tool for melanoma, enabling its commercial use across Europe. The tool integrates with smartphones and dermatoscopes, providing risk scores for melanoma based on dermoscopic image analysis.
2025-05
PharmaShots
AI Medical Technology's Dermalyser Receives European CE Mark Approval for Melanoma Detection
Dermalyser, a stand-alone medical device software designed for smartphones attached to an AI-powered dermatoscope, has received CE mark approval for melanoma detection. Commercialization is set to begin in 2025, with a US market entry aimed for 2027.
2025-05
OEM News
AI Medical Technologies Receives Approval for AI Melanoma Thickness Trial
Swedish AI Medical Technologies has received approval for a clinical trial to further validate Dermalyser's performance in accurately determining melanoma thickness using dermoscopy images. The trial is expected to conclude in Q4 2025.
2024-10
OncLive
AI Support Tool Demonstrates Detection Utility for Melanoma at Primary Care Practices
Dermalyser, an artificial intelligence-based clinical decision support tool, showed high diagnostic accuracy in detecting cutaneous melanoma in a primary care setting, according to a study published in the British Journal of Dermatology. The smartphone app uses AI to analyze dermoscopic images taken by a primary care physician.
2024-05
AI Medical Technology
New Swedish clinical study published in the British Journal of Dermatology demonstrates superiority of AI-algorithm guided melanoma diagnosis
Results from a prospective, multicentre clinical trial published in the British Journal of Dermatology showed that Dermalyser, a smartphone-based diagnostic decision support system, significantly improves melanoma detection rates. Dermalyser achieved remarkable sensitivity and specificity values of 95% and 85%, respectively.
2024-03
British Journal of Dermatology
Evaluation of an artificial intelligence-based decision support for the detection of cutaneous melanoma in primary care: a prospective real-life clinical trial
A prospective real-life clinical trial was conducted to assess the diagnostic performance of the smartphone app Dermalyser, an AI-based decision support tool, to detect melanoma. The study was performed in accordance with STARD 2015 guidelines and approved by the Swedish Medical Products Agency and the Swedish Ethical Review Authority.
2024-07

Videos

Product demos, reviews, and walkthroughs for Dermalyser.

View all on YouTube

Frequently Asked Questions

Dermalyser is a smartphone application that, when used with a compatible dermatoscope, provides AI-driven decision support for evaluating suspected melanomas. Physicians can capture an image of a skin lesion with the app and receive an immediate analysis to aid in their diagnostic process.
Dermalyser is CE-marked as a Class IIa medical device software under MDR (EU) 2017/745, signifying its adherence to European health, safety, and performance standards. The company anticipates FDA 510(k) clearance for the US market by 2027.
Dermalyser is intended for suspected melanomas and should not be used on patients under 18, ulcerated or open lesions, lesions outside the 2mm-2cm size range, or on mucous membranes, under nails, on palms/soles, near eyes, tattooed skin, or previously biopsied lesions. It has been validated for Fitzpatrick skin types I-IV.
Clinical studies indicate Dermalyser achieved an AUROC of 0.960 for melanoma detection, with 95.2% sensitivity and 84.5% specificity, and 100% sensitivity for invasive melanomas. This performance has been shown to surpass expert dermatologists (AUROC 0.85) and general practitioners (AUROC 0.70).
Several AI dermatology tools exist, such as DermaSensor (FDA cleared for three top skin cancers), SkinVision, and VisualDx. Dermalyser differentiates itself as a CE-marked decision support tool specifically for melanoma, demonstrating superior sensitivity and specificity in clinical trials compared to other AI tools and human assessment.
While specific pricing details are not publicly available, Dermalyser is marketed to offer significant cost savings, with studies suggesting up to a 56% reduction in clinical costs. These savings are attributed to improved patient flow, fewer unnecessary referrals, and reduced excisions of benign lesions.
Dermalyser is explicitly designed as a decision-support tool for licensed healthcare professionals and does not replace the expertise of a dermatologist. The final diagnosis and clinical decision-making always remain the responsibility of the physician.

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Suggest an Edit → | Last Verified: 2026-04-30 | First Added: 2026-04-30
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