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Sign in to claim this brandNEUROPHET Inc.
South Korea·KR-MF-000019879
Last updated May 30, 2026
What NEUROPHET Inc. makes
NeuroPhet Inc. develops software applications for processing and analyzing radiology images, including DICOM-based tools for medical imaging workflows. Their portfolio includes solutions for quantitative analysis in PET imaging and automated processing of brain scans, such as Neurophet SCALE PET and Neurophet AQUA variants, designed for clinical and research use.
The company’s products are authorised as Class II and Class IIa medical devices under global regulatory frameworks, with listings in the EU’s eudamed database, FDA’s 510(k) and UDI registries. These devices are intended for use in diagnostic imaging and are governed by standards applicable to their respective risk classifications.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Neurophet Inc. manufacture?
Neurophet Inc. develops software applications for processing and analyzing radiology images, including DICOM-based tools for medical imaging workflows. Their portfolio includes solutions for quantitative analysis in PET imaging and automated processing of brain scans, such as Neurophet SCALE PET and Neurophet AQUA variants.
Where is Neurophet Inc. based?
Neurophet Inc. is based in South Korea (KR), as indicated by the country information provided in the device data.
Which regulatory registries list Neurophet's devices?
Neurophet's devices are listed in the EU's eudamed database, the FDA's 510(k) registry, and the FDA's UDI (Unique Device Identification) registry, as specified in the device data.
How are Neurophet's medical devices classified?
Neurophet's devices are classified as Class II and Class IIa medical devices under global regulatory frameworks, with these classifications reflecting their risk level and the applicable regulatory standards for their intended diagnostic imaging use.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- South Korea
- Address
- 12F-15F, 314, Gangnam-daero, Seoul, South Korea
- Website
- www.neurophet.com
- —
- —
- [email protected]
- Phone
- +82 2 6954 7971
- PRRC Contact
- Yongwoo Cho
- EUDAMED SRN
- KR-MF-000019879
- FDA FEI Number
- —
- DUNS Number
- 694626491
Catalogue (8)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Neurophet AQUA | 3.1 | FDA UDI | Class II | Active |
| Neurophet AQUA | 3.0 | FDA UDI | Class II | Active |
| Neurophet SCALE PET | 1.2 | FDA UDI | Class II | Active |
| Neurophet SCALE PET | K252563 | FDA 510(k) | Class II | Active |
| Neurophet AQUA AD Plus | K252496 | FDA 510(k) | Class II | Active |
| Neurophet SCALE PET | K221405 | FDA 510(k) | Class II | Active |
| Neurophet AQUA (V3.1) | K242215 | FDA 510(k) | Class II | Active |
| En_neurophet Aqua V1.0 | EN_NEUROPHET AQUA V1.0 | EUDAMED | Class IIa | Active |
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