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VIEW-M TECHNOLOGY CO., LTD.

US

Last updated May 24, 2026

Part of View-M Technology

What VIEW-M TECHNOLOGY CO., LTD. makes

VIEW-M Technology Co., Ltd. manufactures manually-adjusted lensmeters that operate on line power, including automated models designed for optical measurements. These devices are primarily used in eye care settings to measure the optical power of lenses, aiding in prescription verification and fitting accuracy.

The company’s products fall under Class I regulatory classification in the U.S., listed in the FDA’s Unique Device Identifier (UDI) database. The portfolio is regulated under the FDA’s medical device authorities, with devices subject to compliance requirements for Class I devices.

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 VIEW-M Technology Co., Ltd. manufacture?

VIEW-M Technology Co., Ltd. specializes in manually-adjusted lensmeters that run on line power. These devices include automated models used in eye care settings to measure the optical power of lenses, helping ensure accurate prescription verification and lens fitting. The company’s focus is on optical measurement tools for clinical use.

Where is VIEW-M Technology Co., Ltd. based?

VIEW-M Technology Co., Ltd. is headquartered in the United States. The company’s location influences its regulatory compliance framework, particularly under U.S. medical device authorities.

Which regulatory registries list VIEW-M Technology Co., Ltd.’s devices?

VIEW-M Technology Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for Class I devices, which are subject to specific U.S. regulatory requirements.

How are VIEW-M Technology Co., Ltd.’s devices classified under U.S. regulations?

VIEW-M Technology Co., Ltd.’s devices fall under Class I regulatory classification in the U.S. This classification is assigned based on the risk profile of manually-adjusted lensmeters and automated lensmeters, which are considered low-risk and generally exempt from strict pre-market approval processes, though they still meet compliance standards.

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

Information

Country
US
Address
—
Website
marco.com
LinkedIn
—
Facebook
—
Phone
+19046429330
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
557821283

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Auto Lensmeter VLM-2400
FDA UDI
Class IActive
Auto Lensmeter ALM-1P
FDA UDI
Class IActive

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