Complira
Complira is a security control plane that unifies telemetry from 30+ security tools, normalizes risk across AI-assisted and human-written code, and enforces release-ready governance. The platform translates scanner findings into product-level risk assessments and gates releases based on policy-aligned security criteria, with compliance mappings for the EU Cyber Resilience Act and FDA 524B requirements.
- Cybersecurity
- Developer Tools
- Regulatory & Compliance Technology
- Software Only
Funding
Founders
Founder details are not available yet.
Product
Problem
Modern software products rely on a fragmented security toolchain, generating siloed telemetry that teams struggle to aggregate and interpret. With the rise of AI-assisted code generation, the attack surface is expanding, yet existing vulnerability management approaches do not uniformly govern AI-generated and human-written code. Regulated industries face mounting compliance mandates, such as the Cyber Resilience Act and FDA requirements, that demand product-level security evidence and release-ready governance.
Solution
Complira is a security control plane for modern software products. It unifies security telemetry from 30+ tools into a single data layer, then normalizes risk across AI-assisted and human-written code to provide a consistent risk picture. The platform translates raw scanner findings into product-level risk assessments, enabling teams to prioritize what matters for release decisions. It enforces release-ready governance by gating releases based on policy-aligned security criteria, ensuring only compliant code ships to production. Complira maintains cryptographic resilience readiness, addressing post-quantum cryptography considerations as attack surfaces evolve. The platform is designed for regulated and high-trust environments, providing a centralized view of security posture across the entire software development lifecycle.
Target Audience
Complira serves healthcare and life sciences companies building FDA 524B-regulated medical devices and AI-based software as a medical device (SaMD), connected product manufacturers in the EU subject to the Cyber Resilience Act, and enterprise software teams developing high-trust applications.
Features
- Unifies security telemetry from 30+ tools, including scanners, vulnerability management systems, and AI code assistants
- Normalizes risk across AI-generated and human-written code with equal governance rigor
- Product-level risk translation that converts scanner-level findings into business-relevant risk metrics
- Release gating and governance enforcement that blocks non-compliant releases based on security policies
- Cryptographic resilience monitoring with post-quantum cryptography awareness for evolving threat landscapes
- Compliance mappings for the EU Cyber Resilience Act (CRA) and FDA 524B requirements for medical device software