Healthcare
Electronics
Engineering
You have the clinical problem. We have the engineers. Tell us what you need — we handle everything from PCB to app to certification.
The Challenge
Every Clinical Breakthrough Starts With a Device That Doesn't Exist Yet.
Off-the-shelf hardware doesn't fit your workflow. Generic platforms can't meet your compliance requirements. Assembling five vendors to ship one device costs you two years you don't have.
We exist for this. One team. Every layer. Hardware, firmware, software, AI, and regulatory — under one roof, no handoffs.
We've built patient monitoring badges, wandering prevention systems, hospital asset trackers, nurse call hardware, and point-of-care diagnostics. If it belongs in a clinical environment, we can build it.
Tell Us the Problem. We'll Build the Device.
The items below are examples. If it belongs in a clinical environment, we engineer it.
Hardware & Device Design
Electronics Design →Custom PCBs to IEC 60601-1 safety requirements — isolated power, patient-applied part classifications, and EMC compliance. Every design starts with the regulatory end-state in mind.
Firmware & Embedded Systems
Firmware Development →RTOS firmware (FreeRTOS, Zephyr) following IEC 62304 guidance. Secure boot, encrypted storage, OTA updates — built for real device fleets, not just prototypes.
Software, AI & Cloud
Software Development →iOS/Android apps, HIPAA-compliant APIs, real-time dashboards, and AI for fall risk and vital sign anomaly detection. Patient data security baked in from the first commit.
Compliance & Certification
Regulatory Support →510(k) technical packages, IEC 62304 records, FCC/CE/IC certification. We design for the regulatory end-state from day one — not retrofitted at submission.
Technology Stack
Platforms We Build Medical Devices On
Deep expertise on the platforms that matter in medical device and hospital system development.
Why Teams Build With Ankh
Everything In-House. No Handoffs.
Hardware, firmware, software, AI, compliance docs — one team owns it all. No subcontractors receive your IP. No scope gaps. Full accountability, end to end.
FDA Documentation Experience
We've supported 510(k) pre-submissions for Class II devices. We design with FDA guidance in mind from day one — not retrofitted at submission.
HIPAA-Aware Architecture by Default
Encrypted transport, data minimization, role-based access, and audit logging — baked into every system from the first commit. Not an afterthought.
Prototype to Production
We don't vanish after the prototype. DFM reviews, manufacturer qualification, sustaining engineering — we stay accountable until your device ships reliably at volume.
Describe the Problem. We Handle the Rest.
Startup, hospital system, or OEM — if you can describe the clinical problem, we can build the device. Hardware, firmware, app, cloud, and certification. Under one roof.
Talk to an EngineerHave a Clinical Problem? Let's Solve It.
Tell us what patients need. We build the hardware, write the firmware, ship the app, and navigate certification — whatever the problem.
Get in Touch