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Medtronic

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medtronic.com·Medtronic plc·Galway, IE·founded 1949·95000+ employees·updated 2026-08-25·revision 1

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Global healthcare technology company that designs, manufactures, and sells medical devices and therapies, including cardiac devices, surgical robotics, surgical tools, and patient monitoring systems, for more than 70 health conditions.

Offerings

6 listed

Hugo RAS System

#hugo-ras

Modular robotic-assisted surgery platform. FDA-cleared in the US for urologic procedures (prostatectomy, nephrectomy, cystectomy); used in 30+ countries outside the US.

hardwareManufacturer

Pricing envelope

—Not statedPrice filters return this as unknown.

Certifications

fda_510kFDA 510(k)third-party · U.S. Food and Drug Administration (FDA)

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“FDA has cleared the Hugo™ robotic-assisted surgery (RAS) system for use in urologic surgical procedures.”https://news.medtronic.com/2025-12-03-Medtronic-announces-FDA-clearance-of-Hugo-TM-robotic-assisted-surgery-system-for-urologic-surgical-proceduresretrieved 2026-08-25 · extracted

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Stealth AXiS System

#stealth-axis

Integrated planning, navigation, and robotics platform for spine surgery with LiveAlign real-time motion tracking. FDA-cleared for spine procedures in the US.

hardwareManufacturer

Pricing envelope

—Not statedPrice filters return this as unknown.

Certifications

fda_510kFDA 510(k)third-party · U.S. Food and Drug Administration (FDA)

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“cleared for spine procedures in the United States, with an underlying architecture designed to support future cranial and ENT applications”https://news.medtronic.com/2026-02-13-Medtronic-receives-FDA-clearance-for-Stealth-AXiS-TM-surgical-system,-first-integrated-planning,-navigation-and-robotics-platform-for-spine-surgeryretrieved 2026-08-25 · extracted

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Affera Mapping and Ablation System with Sphere-9 Catheter

#affera-mapping-ablation

All-in-one high-density mapping and dual-energy (pulsed field/RF) ablation system with Sphere-9 catheter; FDA-approved for persistent AFib and atrial flutter.

hardwareManufacturer

Pricing envelope

—Not statedPrice filters return this as unknown.

Certifications

fda_pmaFDA PMAthird-party · U.S. Food and Drug Administration (FDA)

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“Medtronic receives FDA approval of Affera™ Mapping and Ablation System and Sphere-9™ Catheter”https://news.medtronic.com/2024-10-24-A-new-paradigm-in-electrophysiology-Medtronic-receives-FDA-approval-of-Affera-TM-Mapping-and-Ablation-System-and-Sphere-9-TM-Catheterretrieved 2026-08-25 · extracted

ceCE markingself-declared

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“received CE Mark in March 2023 and was approved in Australia in September 2024”https://news.medtronic.com/2024-10-24-A-new-paradigm-in-electrophysiology-Medtronic-receives-FDA-approval-of-Affera-TM-Mapping-and-Ablation-System-and-Sphere-9-TM-Catheterretrieved 2026-08-25 · extracted

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Micra Leadless Pacemaker

#micra

Leadless transcatheter pacemaker implanted inside the heart, less than one-tenth the size of traditional pacemakers. Median battery life up to 17 years.

hardwareManufacturer

Pricing envelope

—Not statedPrice filters return this as unknown.

Certifications

fda_pmaFDA PMAthird-party · U.S. Food and Drug Administration (FDA)

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“received U.S. Food and Drug Administration (FDA) approval of its Micra™ AV2 and Micra™ VR2”https://news.medtronic.com/2023-05-01-Medtronic-receives-FDA-approval-for-its-next-generation-Micra-leadless-pacing-systemsretrieved 2026-08-25 · extracted

Product page →

Evolut TAVR System

#evolut-tavr

Supra-annular, self-expanding transcatheter aortic valve replacement system for severe aortic stenosis, indicated across surgical-risk categories including low-risk.

hardwareManufacturer

Pricing envelope

—Not statedPrice filters return this as unknown.

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BrainSense Adaptive DBS

#brainsense-adaptive-dbs

Closed-loop deep brain stimulation feature that self-adjusts therapy in real time to a patient's brain activity; used with Percept implantable neurostimulators for Parkinson's disease.

hardwareManufacturer

Pricing envelope

—Not statedPrice filters return this as unknown.

Certifications

fda_pmaFDA PMAthird-party · U.S. Food and Drug Administration (FDA)

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“announces U.S. Food and Drug Administration (FDA) approval of BrainSense™ Adaptive deep brain stimulation (aDBS) and BrainSense™ Electrode Identifier (EI)”https://news.medtronic.com/2025-02-24-Medtronic-earns-U-S-FDA-approval-for-the-worlds-first-Adaptive-deep-brain-stimulation-system-for-people-with-Parkinsonsretrieved 2026-08-25 · extracted

Product page →

Who it is for

RegionsWorldwide

Who the company says it sells to. These regions are not an availability filter; the service area is.

Facts on this page were generated from public sources and have not been reviewed by Medtronic.

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