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FDA Breakthrough Device Designation

Kite Health achieved a major milestone over the weekend by securing Breakthrough Device Designation from the FDA for its innovative pressure monitoring technology. This designation signifies that the FDA recognizes the potential of Kitea's technology to significantly improve the management of chronic health conditions.

For Kitea, this breakthrough designation is a game-changer. It accelerates the development and regulatory review process, potentially bringing their life-saving technology to market faster. This recognition is a testament to Kitea's groundbreaking work and positions them as a leader in the global medical device industry.




© 2023 Kitea Health Ltd


New Zealand
Level 6, 70 S
ymonds Street

Grafton, Auckland 1010, New Zealand 

+64 9 300 3299

United States of America

2140 South Dupont Hwy

Camden, 19934 Delaware, USA
+1 302 336 8883

 

The Kitea System is not currently approved for clinical use.

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