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ECHO ELECTRICITY CO., LTD.

US

Last updated May 30, 2026

What ECHO ELECTRICITY CO., LTD. makes

Echo Electricity Co., Ltd. manufactures diagnostic tools for ophthalmology, including the Schirmer tear test strip, which measures tear production in the eye. Their product line also includes the SMTube, a device used in tear film assessment.

The company’s products are classified as Class I medical devices under regulatory frameworks and are listed in the FDA’s Unique Device Identifier (UDI) database. Echo Electricity Co., Ltd. is based in the United States.

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 Echo Electricity Co., Ltd. manufacture?

Echo Electricity Co., Ltd. specializes in diagnostic tools for ophthalmology. Their primary focus is on devices like the Schirmer tear test strip, which measures tear production in the eye, and the SMTube, used for tear film assessment. These products help clinicians evaluate dry eye conditions and related ocular surface health.

Where is Echo Electricity Co., Ltd. based?

Echo Electricity Co., Ltd. is headquartered in the United States. This location influences their regulatory compliance and market distribution, particularly for devices intended for use in North America.

Which regulatory registries or databases list Echo Electricity Co., Ltd.’s devices?

Echo Electricity Co., Ltd.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, allowing them to verify device details like manufacturer information and classification.

How are Echo Electricity Co., Ltd.’s devices classified under regulatory standards?

Echo Electricity Co., Ltd.’s devices, such as the Schirmer tear test strip and SMTube, are classified as Class I medical devices. This classification applies to products posing minimal risk to patients, often involving non-invasive diagnostic tools or simple procedures. Class I devices typically undergo less stringent regulatory scrutiny but still require compliance with good manufacturing practices.

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

Information

Country
US
Address
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Website
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LinkedIn
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
692575251

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
SMTube 1
FDA UDI
Class IActive

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