Press Releases July 20, 2026 04:00 PM

Gentherm Medical Receives FDA Clearance for ThermAffyx™ Patient Safety System

Gentherm Gains FDA Clearance for Innovative ThermAffyx™ Patient Safety System Targeting Robotic Surgeries

By Ajmal Hussain
Share
Twitter Reddit Facebook LinkedIn
THRM

Gentherm has received FDA 510(k) clearance for its ThermAffyx Patient Safety System, a Class II medical device that integrates active patient warming and securement for robotic-assisted surgeries. Product trials start in August 2026, with revenue expected in Q3 2026. This innovation streamlines surgical patient warming and securement, addressing gaps in current warming methods and enhancing patient safety during robotic procedures.

Gentherm Medical Receives FDA Clearance for ThermAffyx™ Patient Safety System
THRM
Summarize with
ChatGPT Perplexity Claude Grok Gemini

Key Points

  • ThermAffyx combines active underbody warming and securement into a single platform for robotic-assisted surgeries, improving patient safety.
  • FDA clearance enables product trials starting August 2026, with commercial launch and revenue expected in Q3 2026.
  • Gentherm leverages its proprietary Carbotex® carbon-fiber heating technology, expanding its temperature management product portfolio and addressing a significant unmet need in healthcare.

NOVI, Mich., July 20, 2026 (GLOBE NEWSWIRE) -- Gentherm, a global market leader of innovative thermal management and pneumatic comfort technologies, announced today it received FDA 510(k) clearance for its patented ThermAffyx™ Patient Safety System. This Class II medical device combines active patient warming, securement and pressure reduction in a single platform designed for the more than 3 million robotic-assisted surgical procedures performed annually worldwide. Product trials at healthcare facilities are scheduled to begin in August, with revenue generation expected to commence in Q3 2026.

Historically, surgical teams have pieced together separate solutions to address warming and securement issues. ThermAffyx simplifies that process by combining two critical patient safety functions into a single system that fits naturally into existing surgical workflows.

Traditional underbody securement pads help prevent patient movement but do not provide active warming. This is especially problematic in robotic procedures and surgeries that require the patient to be tilted in Trendelenburg position. Studies have found that only 17% to 21% of a patient's body surface area may be available for forced-air warming during these procedures, and more than one-quarter of robotic surgery patients are hypothermic in recovery, despite warming interventions.

The ThermAffyx Patient Safety System was developed to address this gap by integrating active underbody warming directly into an anti-slip securement pad. The radiolucent heating element is powered by Gentherm's proprietary Carbotex® carbon-fiber heating technology. This is more than a new warming device. It's a purpose-built patient safety platform designed around the realities of modern robotic surgery. 

The FDA clearance follows Gentherm's 510(k) submission announced earlier this year and represents a significant expansion of the company's patient temperature management portfolio.

About Gentherm
Gentherm (NASDAQ: THRM) is a global market leader of innovative thermal management and pneumatic comfort technologies. Automotive products include Climate Control Seats (CCS®), Climate Control Interiors (CCI™), Lumbar and Massage Comfort Solutions, and Valve Systems. Medical products include patient temperature management systems. The Company is also developing a number of new technologies and products that will help enable improvements to existing products and to create new product applications for existing and new markets. Gentherm has more than 14,000 employees in facilities across 13 countries. In 2025, the company recorded annual sales of approximately $1.5 billion and secured $2.2 billion in automotive new business awards. For more information, go to www.gentherm.com. 

Investor Contact 
Gregory Blanchette
[email protected]
248.308.1702

Media Contacts
Haley Baur
[email protected]
248.289.9711


Risks

  • Potential challenges in adoption and integration of the new system into existing surgical workflows could limit initial market penetration.
  • Competition from other patient warming and securement solutions may impact market share growth potential.
  • Dependence on successful clinical trials and regulatory compliance for sustained commercial success.

More from Press Releases

New Fluke TLPV2 Solar Test Lead Set Eliminates Risky Live-Box Voltage Measurements in Operating PV Systems Jul 21, 2026 CoinShares Unveils UCITS Platform, Expanding Access to Europe's €26.3 Trillion Regulated Fund Ecosystem Jul 21, 2026 Enigmatig Limited Invests in KUNGFULAND, First-Scripted Feature-Length Action-Comedy Singapore and Canada Treaty Co-Production Using Virtual Production Jul 21, 2026 Statement of no intention to make an offer for Brera Holdings plc (the “Company”) Jul 21, 2026 Zoom appoints Carlos Quaderi as Head of APAC to drive next phase of AI-powered growth Jul 20, 2026