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Qurasense, Inc.

United States·US-MF-000052772

Last updated September 17, 2026

What Qurasense, Inc. makes

Qurasense, Inc. manufactures the Q-Pad Test System and Q-Pad Kit, which are medical devices used for testing purposes.

The company's products are classified as Class I and Class II medical devices and are listed in the EU EUDAMED and FDA 510(k) registries. Qurasense is based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does Qurasense, Inc. manufacture?

Qurasense, Inc. manufactures the Q-Pad Test System and Q-Pad Kit, which are medical devices used for testing purposes. These devices are designed to meet specific testing needs in the medical field.

Where is Qurasense, Inc. based?

Qurasense, Inc. is based in the United States. The company operates from this location, where it designs and manufactures its medical devices for distribution and use in various markets.

Which regulatory registries list Qurasense's devices?

Qurasense's devices are listed in the EU EUDAMED and FDA 510(k) registries. These listings indicate that the devices are registered with the respective regulatory authorities for market availability in the EU and US.

How are Qurasense's medical devices classified?

Qurasense's medical devices are classified as Class I and Class II. Class I devices pose minimal risk, while Class II devices require more regulatory controls to ensure their safety and effectiveness.

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

Information

Country
United States
Address
3517, Edison Way, Menlo Park, United States
Website
qvin.com
LinkedIn
—
Facebook
—
Phone
+1 (833) 367-7846
PRRC Contact
Brian Weinberg
EUDAMED SRN
US-MF-000052772
FDA FEI Number
3023949424
DUNS Number
—

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Q-Pad Test System K231465
FDA 510(k)
Class IIActive
Q-Pad Kit QD1.3
EUDAMED
Class IActive

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