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Sign in to claim this brandAccuvein Inc.
US
Last updated May 25, 2026
What Accuvein Inc. makes
Accuvein Inc. manufactures portable, non-powered medical equipment stands designed to support handheld infrared-light vein locators. Their primary product, the AccuVein device, uses infrared technology to visualize veins beneath the skin, aiding in intravenous access procedures.
The company’s products fall under Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. Accuvein Inc. 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 Accuvein Inc. manufacture?
Accuvein Inc. specializes in portable, non-powered medical equipment stands and handheld infrared-light vein locators. Their most well-known product, the AccuVein device, combines these elements to create a system that visualizes veins beneath the skin using infrared technology. This aids healthcare professionals in locating veins for intravenous access procedures.
Where is Accuvein Inc. based?
Accuvein Inc. is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework, as it operates under U.S. medical device regulations.
Which regulatory registries list Accuvein Inc.’s devices?
Accuvein Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.
How are Accuvein Inc.’s devices classified under medical device regulations?
Accuvein Inc.’s devices fall under Class I classification, which is the lowest risk category for medical devices. This classification is typically assigned to devices that pose minimal risk to patients and users, such as simple supports or non-invasive diagnostic tools like infrared vein locators. The classification determines regulatory oversight requirements.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 807920546
Catalogue (5)
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