Scarlet
Scarlet is Europe's only Notified Body specialized in AI and Software as a Medical Device (SaMD), certifying AI medical devices under EU MDR, UK MDR, and ISO standards for AI medical device manufacturers and healthcare startups.
- Company typePrivate
- Founded2020
- HeadquartersLondon, United Kingdom
- Headcount51–100
- GTM typeB2B
- OfferingServices
What Scarlet does
Scarlet is a privately-held Notified Body headquartered in London, founded in 2020, that operates as Europe's only certification body specialized in Software as a Medical Device (SaMD) and AI-based medical devices. Through its operating subsidiaries Scarlet NB B.V. (Netherlands) and Scarlet NB UK Ltd, the company issues conformity assessment certificates under EU MDR (Regulation 2017/745), UK MDR, ISO 13485 (quality management), ISO 27001 (information security), and ISO 42001 (AI management system), covering medical devices from Class Im through Class III. Scarlet positions itself around deep assessor expertise in iterative AI development, enabling AI medical device manufacturers to ship frequent model updates without the certification bottlenecks typical of traditional Notified Bodies.
The company's proprietary Scarlet Application Portal serves as the operational backbone for submissions, compliance data exchange, and ongoing certificate management. Its core products are AI Medical Device Certification Services and a Certificate Transfer Service offering a 4-week migration path from competing Notified Bodies. Revenue is generated through two streams: one-time Initial Certification Fees (typically starting at €100,000 for EU/UK MDR plus ISO 13485) and recurring Annual Service Fees at a €5,000/month equivalent, billed monthly under multi-year contracts. The pricing model is transparent and fixed, with size-based adjustments for SMEs.
Scarlet targets AI medical device manufacturers and healthcare AI startups, primarily in the EU and UK markets, via a sales-led enterprise GTM motion delivered through its website contact forms and scheduled calls. Named customers include Flok Health, Lucida Medical, Skin Analytics, Feebris, Augmedit, Tandem Health, Fraiya, and Floy. The company has raised approximately $26.5M across three funding rounds (2021 seed, 2022 seed extension led by Creandum, 2024 Series A led by Atomico) and operates with 51-100 employees based across the UK, EU, and US.
Scarlet firmographics
Firmographics- Name
- Scarlet
- Legal name
- Scarlet Global Holdings Ltd
- Website
- https://scarlet.cc
- Company type
- Private
- Founded year
- 2020
- Operating status
- Operating
- Headcount range
- 51–100 employees
- Short description
- Scarlet is Europe's only Notified Body specialized in AI and Software as a Medical Device (SaMD), certifying AI medical devices under EU MDR, UK MDR, and ISO standards for AI medical device manufacturers and healthcare startups.
- Ownership category
- akta.pro rank
Scarlet industry classification
Industry- Product category
- Medical Device Certification & Regulatory Compliance Services
- NAICS
- Testing Laboratories and Services (541380)
- SIC
- Services-Testing Laboratories (8734)
- akta.pro primary industry
- DTx/SaMD Regulatory, Quality & Compliance Software (QMS/ISO/FDA) (HLACANAN)
- akta.pro secondary industry
- Regulatory Readiness & Audit Automation (e.g., EU AI Act, NIST AI RMF, ISO/IEC 42001) (HDAAAMAE)
Keywords
Where Scarlet is headquartered
LocationHeadquarters
- HQ city
- London
- HQ country
- United Kingdom
- HQ region
- Europe
Offices1 record
Markets served
Scarlet business model
Business model- GTM type
- B2B
- Offering type
- Services
- Cost components
- Personnel, Technology or R&D, Operations, Marketing or Sales, Others
Revenue model
- Initial Certification Fees: One-off fees covering assessment and decision for initial certificate. Paid partially at service start and in full once Initial Application has been submitted and accepted. Calculated based on scope of certificate sought (certificate type, organization size, product scope, risk class). Typically starts from €100,000 for EU or UK MDR plus ISO 13485.
- Annual Service Fees: All-inclusive ongoing service fees covering product updates and surveillance activities. Paid in monthly installments from service start. Covers all maintenance activities including audits, change request processing, and support for the lifetime of the certificate. Calculated based on scope of ongoing services, typically starting at €5,000 per month equivalent.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| One time/ perpetual license | Multi-year contract | Initial Certification Fee - One-time assessment fee |
| Subscription | Monthly | Annual Service Fee - Ongoing certification maintenance |
Go-to-market motion2 records
Distribution channels2 records
Marketing channels5 records
Scarlet product offering
Product offeringCore offering
Scarlet is a Notified Body that provides conformity assessment and certification services for AI-based medical devices and Software as a Medical Device (SaMD) under EU MDR, UK MDR, ISO 13485, ISO 27001, and ISO 42001. The offering is purpose-built for AI manufacturers needing iterative model updates, with a specialized application portal, remote audits, transparent fixed-fee pricing, and a streamlined 4-week transfer process for certificates issued by other Notified Bodies.
Product overview
Scarlet is the only Notified Body specialized in AI and Software as a Medical Device (SaMD), offering conformity assessment services for EU MDR, UK MDR, ISO 13485, ISO 27001, and ISO 42001 certifications. The core offering consists of AI Medical Device Certification Services, which provide a streamlined path to certification designed for iterative software development. A supplementary Certificate Transfer Service enables manufacturers to transfer existing certificates in four weeks. Customers interact with the platform through Scarlet's Application Portal. The company also provides LLM Guidance Resources and publishes Customer Stories documenting successful certifications across diverse AI medical device categories including radiology, dermatology, surgery, and diagnostics.
Differentiator
Problem solved
Functional benefit
Products and services
- AI Medical Device Certification Services Conformity assessment services for AI medical devices and Software as a Medical Device (SaMD) under EU MDR, UK MDR, ISO 13485, ISO 27001, and ISO 42001, covering Class Im, IIa, IIb, and III devices, with assessment processes designed for iterative AI model updates and frequent software releases. Targeted at AI medical device manufacturers seeking EU and UK market access.
- Certificate Transfer Service Dedicated transfer service for manufacturers already certified by another Notified Body, providing a customized transfer plan aligned to existing surveillance schedules and a streamlined 4-week timeline for EU MDR, UK MDR, and/or ISO 13485 certificates. Targets manufacturers dissatisfied with timelines or AI expertise at their current body.
Quantifiable outcome
- 14 weeks to EU MDR certification for AI physiotherapy device (Flok Health)
- +5 more outcomes
Companies that use Scarlet
Customer profileNamed customers10 records
Segments3 records
Ideal customer profiles2 records
Scarlet technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature4 records
Scarlet partnerships and signals
Strategic signalScale indicators3 records
Recent moves7 records
Expansion highlights5 records
Scarlet competitors and assessment
Company assessmentBroad incumbents
- BSI Group: BSI is one of the largest and longest-established Notified Bodies in the UK/EU for medical devices, including SaMD and AI-enabled devices. It is a direct comparator because Scarlet's former BSI CEO (Howard Kerr) is on its advisory bench, and BSI is the established player Scarlet is most directly taking share from in AI/SaMD certification.
- TÜV SÜD: TÜV SÜD is a major German-headquartered Notified Body designated under EU MDR with broad medical device certification capabilities, including digital health and software. Comparable to Scarlet as a regulated conformity assessment body for medical devices, but operating across a much broader portfolio of standards and industries.
- TÜV Rheinland: TÜV Rheinland is a global testing, inspection, and certification organization with a designated Notified Body under EU MDR. Comparable to Scarlet in the conformity assessment process for medical devices but as a much larger generalist serving multiple industries and standards beyond SaMD/AI.
- DEKRA: DEKRA is a large European testing and certification organization expanding into medical device certification, including SaMD. It competes with Scarlet as a notified/regulated assessment body for medical devices but from a much broader testing, inspection, and certification portfolio.
- Eurofins Scientific: Eurofins is a large testing services group that has expanded into medical device testing and certification-adjacent services. Comparable to Scarlet in providing regulated testing/assessment services to medical product manufacturers, though Eurofins is much broader and not specifically a Notified Body for SaMD.
- Intertek Group: Intertek is a global assurance, inspection, and product testing company with medical device testing services. Comparable to Scarlet in providing independent third-party assessment services that support regulatory market access, but as a diversified generalist across many product categories.
- SGS Group: SGS is one of the world's largest testing, inspection, and certification companies, with medical device certification capabilities. Comparable to Scarlet as a regulated third-party conformity assessment provider, though at much larger scale and broader industry coverage.
- Element Materials Technology: Element provides testing and certification services including for medical devices and life sciences. Comparable to Scarlet as a regulated testing/certification services provider to manufacturers seeking market access, though Element is heavily weighted toward materials and product testing rather than SaMD specialization.
Direct peers
- NSAI (National Standards Authority of Ireland): NSAI operates a Notified Body for medical devices under EU MDR. It is comparable to Scarlet as a smaller, designated Notified Body competing in the same medical device conformity assessment market in Europe, though with less AI/SaMD specialization.
Emerging players
- Nelson Labs (Sotera Health): Nelson Labs provides laboratory testing services specifically for the medical device and pharmaceutical industries. Comparable to Scarlet in serving medical device manufacturers seeking third-party testing/certification support, though focused on lab-based sterility and biocompatibility testing rather than software/AI conformity assessment.
Market position
Strengths4 records
Weaknesses4 records
Competitive moat5 records
Key risks5 records
Key highlights6 records
Customer concentration
Scarlet social profiles
Digital presenceScarlet compliance and trust
Trust signalCompliance5 records
Scarlet financial estimates
Financial estimateRevenue estimate
Valuation estimate
Scarlet leadership team
Management profileNumber of profiles
Profiles10 records
Scarlet subsidiaries and ownership
Company hierarchySubsidiaries2 records
Scarlet funding detail
Funding detailFunding overview
Funding rounds3 records
Investors4 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Scarlet M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Scarlet
What does Scarlet do?
Scarlet is a Notified Body that provides conformity assessment and certification services for AI-based medical devices and Software as a Medical Device (SaMD) under EU MDR, UK MDR, ISO 13485, ISO 27001, and ISO 42001. The offering is purpose-built for AI manufacturers needing iterative model updates, with a specialized application portal, remote audits, transparent fixed-fee pricing, and a streamlined 4-week transfer process for certificates issued by other Notified Bodies.
Is Scarlet a public or private company?
Scarlet is a private company. It is classified as venture growth investor backed and is currently operating.
When was Scarlet founded?
Scarlet was founded in 2020. It employs 51 to 100 people.
Where is Scarlet based?
Scarlet is headquartered in London, United Kingdom, in the Europe region.
How does Scarlet make money?
Two revenue lines are on record. Initial Certification Fees are the primary driver. The others are annual Service Fees.
Who are Scarlet's main competitors?
Broad incumbents on record are BSI Group, TÜV SÜD, TÜV Rheinland, DEKRA, Eurofins Scientific, Intertek Group, SGS Group and Element Materials Technology. NSAI (National Standards Authority of Ireland) is listed as a direct peer. Nelson Labs (Sotera Health) is listed as an emerging player.
Does Scarlet have an API?
No public API is recorded for Scarlet.
What industry is Scarlet in?
Scarlet's product category is Medical Device Certification & Regulatory Compliance Services. Its primary akta.pro industry code is HLACANAN, DTx/SaMD Regulatory, Quality & Compliance Software (QMS/ISO/FDA), with a secondary code of HDAAAMAE, Regulatory Readiness & Audit Automation (e.g., EU AI Act, NIST AI RMF, ISO/IEC 42001). Its NAICS code is 541380 and its SIC code is 8734.