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Generate Embedded SBOM for C/C++

Trusted by security and compliance teams at 100+ regulated companies in

MedTech

SAMD

AISaMD

FinTech

Energy

eSports

Consumer SaaS

MedTech

Audit-ready SBOM. With every build.

Interlynk automates the full SBOM lifecycle: generate, ingest, enrich, monitor, and share. Built for teams shipping under FDA 524B, EU CRA, NIS2, DORA, and PCI DSS 4.0.

Two business professionals reviewing cybersecurity data on a laptop, surrounded by security and compliance icons.

INDUSTRIES

SBOM compliance for regulated industries.

Healthcare

Financial Institutions

Government

Healthcare cybersecurity concept showing a professional interacting with secure medical data dashboards and encryption visuals.

Healthcare: FDA 524B SBOM

Medical device makers must now ship an SBOM with every premarket submission under FDA Section 524B, or risk a refuse-to-accept before review begins. Interlynk generates submission-ready SBOMs tied to the exact device build, tracks component vulnerabilities across the product lifecycle, and keeps your evidence audit-ready for FDA and global regulators.

Healthcare

Financial Institutions

Government

Healthcare: FDA 524B SBOM

Healthcare

Financial Institutions

Government

Healthcare

Secure medical device software and

streamline global regulatory

compliance.

PLATFORM

From premarket submission under Section 524B to postmarket vulnerability management, Interlynk produces the SBOM evidence the FDA expects, tied to the device you actually shipped.

The whole SBOM lifecycle. One platform.

Automated SBOM Management

Automate the creation and management of Software Bills of Materials (SBOMs) to ensure transparency, compliance, and faster response to vulnerabilities.

Open Source Management

Gain full visibility and control over open-source

components, licensing, and risks while streamlining compliance across your software supply chain.

Gain full visibility and control over open-source components, licensing, and risks while streamlining compliance across your software supply chain.

Supplier Monitoring

Continuously track and assess third-party suppliers for security, compliance, and risk posture to strengthen your overall supply chain resilience.

Post Quantum Readiness

Prepare your systems for the next era of cybersecurity by identifying cryptographic dependencies to meet post-quantum threats.

Gain full visibility and control over open-source

components, licensing, and risks while streamlining compliance across your software supply chain.

COMPLIANCE

From premarket submission under Section 524B to postmarket vulnerability management, Interlynk produces the SBOM evidence the FDA expects, tied to the device you actually shipped.

What the FDA expects, and how Interlynk delivers it.

FDA Cybersecurity Requirements (524B)

Generate the SBOM artifacts FDA expects in premarket submissions — formatted, complete, and traceable to the device build that shipped.

FDA Cybersecurity Requirements (524B)

Generate the SBOM artifacts FDA expects in premarket submissions — formatted, complete, and traceable to the device build that shipped.

Vulnerability Monitoring Across the Supply Chain

Watch every component in every version for new CVEs as they're disclosed. Filter out what doesn't apply with VEX, so your team responds to real risk instead of triaging noise.

Vulnerability Monitoring Across the Supply Chain

Watch every component in every version for new CVEs as they're disclosed. Filter out what doesn't apply with VEX, so your team responds to real risk instead of triaging noise.

Demonstrating Secure-by-Design Practices

Map your SDLC artifacts to FDA's secure-by-design expectations automatically — version control, dependency review, vulnerability response — without rebuilding the evidence trail for every submission.

Demonstrating Secure-by-Design Practices

SBOM Mandates and Documentation Gaps

Close the gap between what your dev team builds and what your regulatory team needs to submit. Interlynk reconciles the two automatically, so nothing gets lost between sprints and submissions.

SBOM Mandates and Documentation Gaps

Close the gap between what your dev team builds and what your regulatory team needs to submit. Interlynk reconciles the two automatically, so nothing gets lost between sprints and submissions.

Managing Patch & Update Expectations

Show FDA your patch posture across the device fleet at any point in time. Prioritize fixes by exploitability, not CVSS alone.

Managing Patch & Update Expectations

Show FDA your patch posture across the device fleet at any point in time. Prioritize fixes by exploitability, not CVSS alone.

Audit & Submission Readiness

One queryable record per device, one click to export. Stop assembling submission packages from spreadsheets the night before they're due.

Audit & Submission Readiness

One queryable record per device, one click to export. Stop assembling submission packages from spreadsheets the night before they're due.

SBOM compliance FAQ

How is Interlynk different from other SBOM tools?

Most SBOM tools stop after generation. Interlynk runs the full lifecycle. We generate SBOMs from your source code in CI/CD. We ingest them from your vendors. We enrich them with vulnerability and license context. We monitor them for new CVEs as they're disclosed. We share them with auditors in any format they ask for. Five steps. One platform. No tool chain to maintain. That's the difference: SBOMs that survive contact with regulators and auditors of FDA 524B, EU CRA, NIS2, DORA, and PCI DSS 4.0 — without your team rebuilding documentation for every release.

Does Interlynk help with CRA, NIS2, DORA, CSCRF, or US federal compliance?

Can I bring my own scanner?

Can I request SBOMs from my vendors through Interlynk?

Can Interlynk generate SBOMs for C & C++ codebases?

Can I shift-left with SBOMs, and does Interlynk support this?

Latest SBOM and compliance guides.

From CMake Build to SBOM: Trusted Firmware-M on STM32H5

Jul 5, 2026

Generating accurate CycloneDX SBOMs for a Trusted Firmware-M build on STM32H5 using lynkctl — driven by the CMake build and linker maps, not source scanning

Why SBOM Management Breaks in Large Enterprises

Jun 30, 2026

Enterprise SBOM management breaks at scale for five predictable reasons. Why generating SBOMs is the easy part, and managing them is where programs fail.

CycloneDX vs SPDX: Choosing an SBOM Format for Regulatory Compliance (2026 Edition)

Jun 23, 2026

CycloneDX vs SPDX: compare the two SBOM formats for regulatory compliance. Current versions, ISO and ECMA certification, tooling, and how to choose.

EU Cyber Resilience Act SBOM requirements based on Germany BSI Technical Guideline TR-03183

SBOM Requirements for the CRA: A Guide to BSI TR-03183

Jun 20, 2026

SBOM Requirements for the CRA: A Guide to BSI TR-03183

From CMake Build to SBOM: Trusted Firmware-M on STM32H5

Jul 5, 2026

Generating accurate CycloneDX SBOMs for a Trusted Firmware-M build on STM32H5 using lynkctl — driven by the CMake build and linker maps, not source scanning

Why SBOM Management Breaks in Large Enterprises

Jun 30, 2026

Enterprise SBOM management breaks at scale for five predictable reasons. Why generating SBOMs is the easy part, and managing them is where programs fail.

CycloneDX vs SPDX: Choosing an SBOM Format for Regulatory Compliance (2026 Edition)

Jun 23, 2026

CycloneDX vs SPDX: compare the two SBOM formats for regulatory compliance. Current versions, ISO and ECMA certification, tooling, and how to choose.

SBOM Requirements for the CRA: A Guide to BSI TR-03183

Jun 20, 2026

SBOM Requirements for the CRA: A Guide to BSI TR-03183

SBOM Strategy & Attestation for OSS Projects: A 2026 Best-Practices Guide

Jun 3, 2026

How open-source projects build an SBOM strategy and attestation model: formats, CI automation, signing, VEX, and CRA/FDA/NIS2 mapping. 2024–2026 best practices.

From SCA to SBOM: A Practical Guide to Migrating

May 30, 2026

Your SCA tool already builds an SBOM, then locks it in a console. A practical guide to migrating to an open, SBOM-first workflow with no coverage gap.

Q-Day Just Got Closer: What Recent Quantum Breakthroughs Mean for Your Industry

May 25, 2026

Recent quantum computing breakthroughs have moved the PQC deadline earlier. What financial services, critical infrastructure, and medical device leaders need to do now.

Interlynk Medical Device Cybersecurity MITRE 2026

Medical Device Cybersecurity 2026: The MITRE Report Decoded

May 8, 2026

Decoding MITRE's April 2026 medical device cybersecurity report — what its findings mean for manufacturers, SBOMs, and FDA-aligned risk management.

Trusted by security and compliance teams at 100+ regulated companies