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Uptake Medical Technologies, Inc.

United States·US-MF-000032755

Last updated September 18, 2026

About

Uptake Medical® Technology Inc. is a medical device company based in San Jose, CA, USA. Uptake Medical is dedicated to improving the lives of patients suffering from pulmonary disease with vapor ablation.

From the manufacturer's own website. Source

What Uptake Medical Technologies, Inc. makes

Uptake Medical Technologies, Inc. manufactures devices for vapor ablation procedures, including the InterVapor Generator—a system for delivering controlled vapor—and associated components such as the InterVapor Personalized Procedure Program (IP3), drain bags, and catheters. These products are designed to assist in pulmonary interventions, particularly for patients with respiratory conditions.

The company’s devices are classified under EU regulations as Class I, Class IIa, and Class IIb, with listings maintained in the EUDAMED database. The manufacturer is headquartered in San Jose, California, USA.

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 Uptake Medical Technologies, Inc. manufacture?

Uptake Medical Technologies, Inc. specializes in devices for vapor ablation procedures in pulmonary medicine. Their portfolio includes the InterVapor Generator—a system for delivering controlled vapor—and complementary components like the InterVapor Personalized Procedure Program (IP3), drain bags, and catheters. These devices are designed to support interventions for patients with respiratory conditions by enabling precise vapor-based treatments.

Where is Uptake Medical Technologies, Inc. based?

The company is headquartered in San Jose, California, USA. This location serves as its primary operational base for manufacturing and developing its medical devices.

Which regulatory registries list Uptake Medical Technologies, Inc.’s devices?

Uptake Medical Technologies, Inc.’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This listing is required for transparency and traceability under EU regulations.

How are Uptake Medical Technologies, Inc.’s devices classified under EU regulations?

The company’s devices fall into three classification categories under EU regulations: Class I, Class IIa, and Class IIb. The classification determines the level of scrutiny and regulatory requirements for each device, with higher classes (e.g., Class IIb) typically involving more rigorous evaluation due to higher risk.

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

Information

Country
United States
Address
125, Nicholson Lane, San Jose, United States
LinkedIn
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Facebook
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Phone
949.440.1800
PRRC Contact
Antoinette Clay
EUDAMED SRN
US-MF-000032755
FDA FEI Number
—
DUNS Number
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Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
InterVapor Generator UM-GEN-100
EUDAMED
Class IIbActive
InterVapor® Personalized Procedure Program (IP3®) UM-IP3-100
EUDAMED
Class IIbActive
InterVapor Drain Bag UM-BAG-100
EUDAMED
Class IActive
InterVapor Catheter UM-CTH-100
EUDAMED
Class IIaActive

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