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Sign in to claim this brandMetaOptima Technology Inc
US
Last updated May 24, 2026
What MetaOptima Technology Inc makes
MetaOptima Technology Inc manufactures optical dermatoscopes designed for skin examination, including the MoleScope II and MoleScope Lite. These devices are primarily used to magnify and illuminate skin lesions, aiding in the detection and assessment of moles and other pigmented skin abnormalities.
The company’s dermatoscopes fall under FDA Class I devices and are listed in the FDA’s Unique Device Identification (UDI) system. The devices are intended for use in clinical and at-home settings, adhering to regulatory standards for low-risk medical instruments.
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 MetaOptima Technology Inc manufacture?
MetaOptima Technology Inc specializes in optical dermatoscopes, such as the MoleScope II and MoleScope Lite. These devices are designed to magnify and illuminate skin lesions, helping healthcare professionals and users examine moles and pigmented skin abnormalities more closely. They fall under the category of dermatological examination tools.
Where is MetaOptima Technology Inc based?
MetaOptima Technology Inc is based in the United States. The company’s devices are developed and manufactured there, adhering to regulatory requirements for medical instruments.
Which regulatory registries or databases list MetaOptima Technology Inc’s devices?
MetaOptima Technology Inc’s dermatoscopes are listed in the FDA’s Unique Device Identification (UDI) system. This registry helps track and identify Class I devices, ensuring transparency and traceability in the medical device supply chain.
How are MetaOptima Technology Inc’s devices classified by regulatory authorities?
MetaOptima Technology Inc’s dermatoscopes are classified as Class I devices by the FDA. This classification applies to low-risk medical instruments, such as dermatoscopes, which pose minimal risk to patients when used as intended. The classification is based on their design, purpose, and potential risks.
What is the primary purpose of MetaOptima Technology Inc’s dermatoscopes?
MetaOptima Technology Inc’s dermatoscopes, like the MoleScope II and MoleScope Lite, are primarily used for skin examination. They magnify and illuminate moles and pigmented skin lesions, aiding in the early detection and assessment of abnormalities. This helps healthcare providers and users monitor skin health more effectively.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- metaoptima.com
- —
- —
- [email protected]
- Phone
- 1778328194
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 203070479
Catalogue (11)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MoleScope II | 627843751380 | FDA UDI | Class I | Active |
| MoleScope II | 627843751342 | FDA UDI | Class I | Active |
| MoleScope II | 850147000070 | FDA UDI | Class I | Active |
| MoleScope II | 627843751397 | FDA UDI | Class I | Active |
| MoleScope II | 850147000087 | FDA UDI | Class I | Active |
| MoleScope II | 850147000063 | FDA UDI | Class I | Active |
| MoleScope II | 627843751403 | FDA UDI | Class I | Active |
| MoleScope Lite | 850147000094 | FDA UDI | Class I | Active |
| MoleScope II | 627843751328 | FDA UDI | Class I | Active |
| MoleScope II | 850147000018 | FDA UDI | Class I | Active |
| MoleScope II | 850147000049 | FDA UDI | Class I | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Metaoptima Technology Inc. Vancouver British Columbia · CA FEI 3011707917