DEPLOYDatabase

Robot model

Genesis RMN / GenesisX

Stereotaxis (NYSE American: STXS; headquartered in St.

Manufacturer
Stereotaxis
Form factor
surgical
Maturity
commercial
Lifecycle
active
Deployments
1

Overview

Stereotaxis (NYSE American: STXS; headquartered in St. Louis, Missouri) pioneered Robotic Magnetic Navigation, a distinct surgical-robot modality in which two large external magnets robotically steer a magnetic-tipped catheter inside the heart for catheter-based electrophysiology and cardiac ablation. It is genuinely a robot, with computer-controlled physical actuation of an in-body instrument, but an unusual one whose manipulator is the magnetic field acting on a soft catheter rather than a rigid arm, placing it in a distinct endovascular sub-category rather than the soft-tissue laparoscopic mainstream. Its current-generation Genesis RMN system succeeded the legacy Niobe, the next-generation small-footprint GenesisX received its European CE mark in August 2024 and US FDA 510(k) clearance on November 10, 2025, and the MAGiC magnetic ablation catheter that the system steers received FDA approval on January 6, 2026, with the first US procedure performed at OHSU. The registry records it at commercial maturity, with more than 100 RMN systems installed across about 31 countries, public-company revenue, and GenesisX in early limited launch, and notes that the company signed an agreement to acquire the endovascular-robotics firm Robocath in early 2026. A correction to the dispatch framing: no Stereotaxis product named Mavericks exists in any primary source, and the real third leg of the portfolio is the MAGiC ablation catheter, so Mavericks is not recorded. The figure of more than 140,000 cumulative patients is a company marketing figure, and exact current GenesisX install counts beyond a first installation and limited launch are not verified.

Verified vs. claimed

Maturity stage
commercial(Commercially deployed with revenue-generating operations.)
Verified deployments
1 deployment on file
Sources on file
4 sources, view all

Key facts

Installed base

>100 RMN systems across ~31 countries

CE mark

GenesisX received European CE mark in August 2024

FDA clearance

GenesisX received FDA 510(k) clearance on November 10, 2025

FDA approval

MAGiC ablation catheter received FDA approval on January 6, 2026

Q1 2026 system revenue

$1.3M of $6.3M total revenue

Specs

Notes

Verified: Stereotaxis (NYSE American: STXS; HQ St. Louis MO) pioneered Robotic Magnetic Navigation (RMN) for catheter-based electrophysiology: two external magnets reorient a magnetic-tipped catheter inside the heart. GenesisX got CE mark Aug 2024 + FDA 510(k) Nov 10 2025; the MAGiC ablation catheter got FDA approval Jan 6 2026 (first US procedure at OHSU). Signed an agreement to acquire Robocath (endovascular robotics, Q1 2026)., CORRECTION (dispatch framing): No Stereotaxis product named 'Mavericks' appears in any primary source. The real third leg of the current portfolio is the MAGiC ablation catheter (FDA Jan 2026); 'Mavericks' is a mis-recalled name and is NOT recorded., Modality + maturity: It IS a robot (computer-controlled physical actuation of an in-body instrument), but an unusual one: the 'manipulator' is the magnetic field acting on a soft catheter, not a rigid arm. A distinct sub-category (endovascular/magnetic catheter robotics), not a soft-tissue laparoscopic robot. maturity=commercial (Genesis family long-commercialized; >100 RMN systems across ~31 countries; public-company revenue; GenesisX in early/limited launch)., Claimed but NOT verified: >140,000 cumulative patients (company/marketing figure); exact current GenesisX order/install count beyond 'first installation' + limited launch. Q1 2026 system revenue was small ($1.3M of $6.3M total), reflecting a mature/legacy installed base with GenesisX only beginning to ship.

Products

Genesis RMN (current-gen robotic magnetic navigation, FDA-cleared, succeeded legacy Niobe); GenesisX (next-gen small-footprint RMN, CE Aug 2024, FDA 510(k) Nov 10 2025); MAGiC magnetic ablation catheter (FDA approval Jan 6 2026); plus an imaging system. Niche: electrophysiology / cardiac ablation.

Form Factor

surgical (robotic magnetic navigation: robotically steers magnetic-tipped catheters inside the heart via external magnets)

Fda clearance

FDA 510(k) clearance on November 10, 2025

Clearance body

FDA

Procedure types

catheter-based electrophysiology and cardiac ablation

Data & sources

Press releases

3

Web sources

1

4 sources backing this record.View all →

Pricing

No verified price is on record for Genesis RMN / GenesisX. Physical-AI systems are often sold through enterprise contracts or operated as a service rather than at a public list price.

Deployments (1)

Genesis RMN / GenesisX on the deployment map

Where Genesis RMN / GenesisX is verified operating. Explore the deployment map by place and type.

Recent activity

Every change to this record is dated, sourced, and independently verified where marked.

Full change history →

Deployment-verified media (1)

PRIMARY SOURCE
Courtesy of Stereotaxis

Stereotaxis' introduction of its Genesis Robotic Magnetic Navigation system. This is robotic magnetic navigation for catheter-based cardiac electrophysiology (endovascular), a different modality from laparoscopic surgery.

From deployment: United States

Regulatory filings (2)

Safety record

No incidents on record for Genesis RMN / GenesisX.

Only active incidents are counted. Retracted incidents are excluded from this summary but remain reachable at their canonical URLs.

Sources (4)

  1. https://www.globenewswire.com/news-release/2025/11/10/stereotaxis-genesisx-fda-clearance
  2. https://www.globenewswire.com/news-release/2026/01/06/stereotaxis-magic-catheter-fda
  3. https://www.globenewswire.com/news-release/2026/05/12/stereotaxis-q1-2026-results
  4. https://en.wikipedia.org/wiki/Stereotaxis

Common questions

What is Genesis RMN / GenesisX?
Stereotaxis (NYSE American: STXS; headquartered in St. Louis, Missouri) pioneered Robotic Magnetic Navigation, a distinct surgical-robot modality in which two large external magnets robotically steer a magnetic-tipped catheter inside the heart for catheter-based electrophysiology and cardiac ablation. It is genuinely a robot, with computer-controlled physical actuation of an in-body instrument, but an unusual one whose manipulator is the magnetic field acting on a soft catheter rather than a rigid arm, placing it in a distinct endovascular sub-category rather than the soft-tissue laparoscopic mainstream. Its current-generation Genesis RMN system succeeded the legacy Niobe, the next-generation small-footprint GenesisX received its European CE mark in August 2024 and US FDA 510(k) clearance on November 10, 2025, and the MAGiC magnetic ablation catheter that the system steers received FDA approval on January 6, 2026, with the first US procedure performed at OHSU. The registry records it at commercial maturity, with more than 100 RMN systems installed across about 31 countries, public-company revenue, and GenesisX in early limited launch, and notes that the company signed an agreement to acquire the endovascular-robotics firm Robocath in early 2026. A correction to the dispatch framing: no Stereotaxis product named Mavericks exists in any primary source, and the real third leg of the portfolio is the MAGiC ablation catheter, so Mavericks is not recorded. The figure of more than 140,000 cumulative patients is a company marketing figure, and exact current GenesisX install counts beyond a first installation and limited launch are not verified.
How much does Genesis RMN / GenesisX cost?
Genesis RMN / GenesisX's price is not publicly disclosed. DEPLOY has no verified price on record for Genesis RMN / GenesisX from Stereotaxis. Physical-AI systems like this are often sold through enterprise contracts or operated as a service rather than at a public list price; check the manufacturer for the latest.
Is Genesis RMN / GenesisX actually deployed in the real world?
Yes. Genesis RMN / GenesisX is independently verified in real-world operation on the DEPLOY registry, confirmed at named deployment sites with primary sources: not a concept, render, or demo-only.
Who makes Genesis RMN / GenesisX?
Genesis RMN / GenesisX is made by Stereotaxis, based in St. Louis, MO, USA, founded in 1990.
Where is Genesis RMN / GenesisX deployed?
1 verified deployment of Genesis RMN / GenesisX is on the DEPLOY registry, including at United States.
Methodology: Verified · 4 sources (3 primary) · last reviewed 2026-07-12

Verification posture

Verified

High confidence

Review state

Stable

Last reviewed 2026-07-12

Maturity + lifecycle

Maturity stage: commercial

Lifecycle: active

Architectural position

Cohort: surgical

Sources by quality tier

3
primary-company-ir
Company IR disclosure
1
knowledge-base
Knowledge base

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

Methodology surface for Genesis RMN / GenesisX.

Recent coverage

Genesis RMN / GenesisX in third-party press