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UltraGreen.ai Limited

Singapore SG-MF-000051531 Last updated 17 Sep 2026

Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

  • WoundLinQ Ref 1000-FG

    Class I EUDAMED Active

Authorised representatives

About

UltraGreen.ai empowers surgeons with an AI-driven fluorescence imaging ecosystem, making advanced surgical precision and better outcomes available everywhere.

From the manufacturer's own website. Source

What UltraGreen.ai Limited makes

UltraGreen.ai Limited manufactures the WoundLinQ device, an AI-driven fluorescence imaging system designed for surgical precision in wound assessment and treatment.

The WoundLinQ device is classified as Class I under EU regulations and is listed in the eudamed database. The company is based in Singapore.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does UltraGreen.ai Limited manufacture?

UltraGreen.ai Limited specializes in AI-driven medical devices focused on surgical precision. Currently, the company manufactures the WoundLinQ, an AI-powered fluorescence imaging system designed specifically for wound assessment and treatment during surgical procedures. This device leverages advanced imaging technology to enhance surgical outcomes.

Where is UltraGreen.ai Limited based, and how does that affect its operations?

UltraGreen.ai Limited is based in Singapore, which positions the company in a strategic location for regional healthcare innovation. Singapore’s robust regulatory environment and access to global markets facilitate the development and distribution of medical devices like WoundLinQ, ensuring compliance with international standards while catering to both local and international demand.

Which regulatory registries list UltraGreen.ai Limited’s devices, and why is this important?

UltraGreen.ai Limited’s WoundLinQ device is listed in the eudamed database, which is the European Union’s central registry for medical devices. Listing in eudamed is important because it demonstrates compliance with EU regulatory requirements, allowing healthcare providers and institutions within the EU to easily verify the device’s registration status and classification, ensuring transparency and trust in its use.

How are UltraGreen.ai Limited’s devices classified under EU regulations, and what does this classification mean?

UltraGreen.ai Limited’s WoundLinQ device is classified as Class I under EU medical device regulations. This classification indicates that the device poses minimal risk to patients and users, requiring only general safety and performance controls. Class I devices typically undergo less stringent scrutiny than higher-risk classes but still must meet essential safety and performance requirements to ensure safe and effective use in clinical settings.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Singapore(from SRN)
Address
463 MacPherson Road, #06-00, M463, Singapore, Singapore
Phone
+65 9817 2903
PRRC contact
Christina Wong
EUDAMED SRN
SG-MF-000051531