Medical Device Software and AI Experts

We help companies commercialize and FDA-clear medical device software and AI. Whether you're looking for regulatory consulting, a software partner, cybersecurity support, or a full-service partner—we can help.

Our Services

Our Solutions

Why Innolitics?

  • All we do is medical-device software
  • Developed software for over 70 medical devices since 2012
  • Team has FDA cleared more than 50 SaMD and SiMD products
  • Four AI/ML and image-processing experts on our team, including two PhDs
  • Cybersecurity expertise in threat modeling, security risk management, SBOMs and more

Trusted by emerging startups to category-leading healthcare companies.

Don't take our word for it.

They were proactive, informative, and very well-versed in the regulatory challenges of AI in medical imaging… Unlike competitors, who sometimes take a blanket approach, Innolitics didn't throw the baby out with the bathwater. They recognized the good work already done and built upon it… We reviewed other capable firms, but none showed the same depth of understanding of the rapidly evolving landscape of AI and regulatory requirements. Their proactive stance with the FDA gave us confidence that we were in the right hands, compared to competitors who seemed more reactive.
Dr. Jagi Gill, MD

Dr. Jagi Gill, MD

Founder and Managing Director

Working with Innolitics was a true game-changer for us. Their exceptional expertise in both engineering and regulatory affairs enabled us to speed up our product development and achieve FDA clearance within a year. Innolitics is more than just an engineering firm—they're a trusted partner. I have complete confidence in their technical skills to build things right the first time.
Dr. Steven Rothenberg MD

Dr. Steven Rothenberg MD

Managing Partner

7 weeks to submission and 6 months to FDA clearance. Innolitics delivered exactly what we needed. They took ownership of the entire DHF and 510(k) package—documentation, cybersecurity, risk management, the works. When we hit internal roadblocks, they found ways to keep us moving. When scope decisions needed to be made fast, they made the right calls. Fast, thorough, no surprises, and full service. That's how regulatory consulting should work!
Dr. Peter Killcommons, MD

Dr. Peter Killcommons, MD

CEO MedWeb

We needed a team that would get it done right the first time and independently. As a physician, I was delighted to work with another physician engineer on the team that was able to implement complex clinical workflows with very little input from me or my team. **Innolitics delivered ahead of schedule and exceeded expectations. Every step of the way, Innolitics demonstrated why they’re leaders in medical software development.**
Dr. Mark Rosenberg, DO, MBA, FACEP, FAAHPM, FACHT

Dr. Mark Rosenberg, DO, MBA, FACEP, FAAHPM, FACHT

Co-Founder and Chairman of Retrieve Medical

Our FDA submission deadline was just two weeks away, and we had no software or cybersecurity documentation. We feared we would miss the deadline. Then our regulatory team introduced us to Innolitics. Their team swiftly validated our software and prepared the 15 necessary software and cybersecurity documents. They took a pragmatic approach that truly added value. This rapid timeline would have been impossible to meet without a team deeply knowledgeable in software, cybersecurity, AI/ML, and FDA regulations. In the end, we were able to submit on time! Thank you, Innolitics, for your Herculean efforts!
Andrea Cubitt

Andrea Cubitt

CEO of Dionysus Digital Health

We recently got FDA cleared and Innolitics' responses were absolutely clutch to craft the strategy that finally worked. Unlike other consultants, who wanted us to do more work and spend more money on clinical testing, Innolitics found a path of least resistance using a combination of our existing validation and thoughtful responses to FDA. We received the best Christmas present ever – our 510(k) clearance letter.
Tushar Pandey

Tushar Pandey

CEO at SimBioSys

We’re grateful to Innolitics for their expert help in getting our product 510(k) cleared. Our team was totally focused on other objectives, so we were excited to learn about the Innolitics Fast 510(k) service. Working with them was smooth, and now we have an FDA cleared product!
Rob Lewis

Rob Lewis

CEO of Radical Imaging

I needed a software development partner to write the software, train the AI, and get FDA clearance. An investor once told me that it would take me $5 million and 5 years to get to where we are now. Innolitics got me here 3 years ahead of schedule and $4 million dollars under budget.
Dr. Andrew Smith, MD PhD

Dr. Andrew Smith, MD PhD

Co-Founder at AI Metrics & Chair of Diagnostic Imaging at St. Jude Children's Research Hospital

Companies like yours create medical device software with Innolitics

We've helped develop software and achieve FDA clearance on more than 70 projects since we were founded in 2012

Orthopedic AI/ML SaMD Strategy and Presub

OrthoVentions, a medical device startup accelerator partnering with Hospital for Special Surgery, needed FDA regulatory strategy for Gemini—an AI-powered SaMD platform creating 3D joint models from 2D MRI. After finding two other consultants suboptimal, they chose Innolitics for proactive FDA expertise, pragmatic approach that preserved strong existing work, and strategic project management. Innolitics delivered a robust FDA Pre-Submission on time and within budget. The outcome: "They did what they said they were going to do, and they did it within the budget that they said they were going to do. So there were no surprises."

Read the case study

Dr. Jagi Gill, MD - Radiology

Regulatory StrategyAI/ML
Logo, OrthoVentions

Smile Dx (Dental CADe AI/ML SaMD)

Innolitics partnered with Cube Click to develop Smile Dx, an AI-powered dental diagnostic tool that enhances dentists' ability to detect caries (cavities), periodontal disease (gum disease), and periapical radiolucencies (PARL). The project showcases our engineering expertise through the development of a comprehensive web application with deep learning capabilities, while also demonstrating our regulatory competence by successfully guiding the product through FDA pre-submission and 510(k) submission processes.

Read the case study

Dr. Richard Ricci, DDS, MS, FAGD, Dr. Andrea R. Cambria, DDS, FAGD - Dental

Guided 510(k)Software DevelopmentWeb-AppAI/MLImage Processing510k
Logo, Cube Click, Inc.

RadUnity (FDA Cleared DICOM Workflow Engine)

We implemented a data-intensive DICOM image processing system to aid clinical workflows. We built this as a modern web application for ease of use. We prepared a complete 510(k) submission for the device and obtained FDA clearance. Both engineering and FDA clearance were completed within 14 months, starting from the ground up.

Read the case study

Tim Szczykutowicz, PhD - Radiology

Software DevelopmentFast 510(k)Regulatory StrategyFDA Hold Letter ResponseGuaranteed AI/ML 510(k) Submission in 3 MonthsGuaranteed Strategy, Q-Sub, and BDD in 2 WeeksWeb-AppImage ProcessingDICOM510k
Logo, RadUnity

NSI (Automated Neuroanatomy in Infant brains)

Innolitics partnered with NeuroSpectrum Insights to develop Gyricalc, a diagnostic tool for neurodevelopmental conditions in children as young as two years old. This project showcases our engineering expertise in transforming a research idea into a fully developed web application and highlights our regulatory proficiency in successfully navigating the FDA pre-submission and 510(k) submission processes.

Read the case study

Andrew Stewart - Neurology

Software DevelopmentGuided 510(k)Regulatory StrategyWeb-App510kImage Processing
Logo, NeuroSpectrum Insights, Inc

Body Check (FDA Cleared End to End AI/ML SaMD)

AI/ML engineering and FDA clearance of a radiology AI/ML quantitative imaging SaMD.

Read the case study

Dr. Steven Rothenberg MD - Radiology

Medical Imaging AI DevelopmentSoftware DevelopmentRegulatory StrategyFDA Hold Letter ResponseFast 510(k)FDA CybersecurityAI/ML510kImage Processing
Logo, Body Check

Emergency FDA AI Request Rescue for an AI/ML SaMD Application

Time critical responses to FDA’s concerns with clearance soon after

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Tushar Pandey - Radiology

FDA Hold Letter ResponseAI/ML
Logo, SimBioSys

Fast 510(k) for Breakthrough IVD

Guide an engineering team without FDA experience through a 510(k) for a breakthrough in vitro diagnostic (IVD) platform

Read the case study

VP of Systems R&D - Microbiology

Fast 510(k)Guaranteed AI/ML 510(k) Submission in 3 MonthsGuaranteed Strategy, Q-Sub, and BDD in 2 Weeks510kIVD

Radify Triage Cybersecurity FDA AI Request Response

Rapid response to hold letter with major cybersecurity findings. Clearance 3 months later.

Read the case study

Andrei Migatchev - Radiology

FDA Hold Letter ResponseFDA Cybersecurity510k
Logo, Envisionit Deep AI

Radiology Software Fast 510(k)

Fast 510(k) for a medical image viewer starting with no documentation

Read the case study

Rob Lewis - Radiology

Fast 510(k)Guaranteed AI/ML 510(k) Submission in 3 MonthsGuaranteed Strategy, Q-Sub, and BDD in 2 Weeks510k
Logo, Software Services Firm with First Product

Medical Image Viewer Guided 510(k)

Guide an engineering team without FDA experience through a 510(k) for a medical image viewer

Read the case study

Amr Abodraiaa, Momen Mohamed - Radiology

Guided 510(k)510k
Logo, Rology

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