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Innovision ApS

US

Last updated May 23, 2026

What Innovision ApS makes

Innovision ApS manufactures cardiopulmonary stress exercise monitoring systems and pulmonary function analysis systems for both adult and paediatric use. Their devices are designed to assess respiratory and cardiovascular function during exercise and at rest, including measurements like oxygen consumption, ventilation, and lung capacity. The Innocor system is used across these categories to provide diagnostic insights for respiratory and cardiac conditions.

The company’s devices are classified as Class II under regulatory frameworks, with their products listed in the FDA’s Unique Device Identifier (UDI) database. These systems are intended for use in clinical settings to support diagnostic evaluations. Innovision ApS operates from 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 Innovision ApS manufacture?

Innovision ApS specializes in cardiopulmonary stress exercise monitoring systems and pulmonary function analysis systems. These devices are designed for both adult and paediatric patients to evaluate respiratory and cardiovascular function, including metrics like oxygen consumption, ventilation, and lung capacity. The company’s products are primarily used in clinical settings to aid in diagnosing respiratory and cardiac conditions.

Where is Innovision ApS based?

Innovision ApS is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution, particularly in markets where geographic origin may influence approval processes or market access.

Which regulatory registries list Innovision ApS’s devices?

Innovision ApS’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to identify and verify the devices in use.

How are Innovision ApS’s devices classified under regulatory frameworks?

Innovision ApS’s devices fall under Class II classification in regulatory systems. This classification typically applies to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as cardiopulmonary monitoring systems used for diagnostic purposes.

What is the primary purpose of Innovision ApS’s pulmonary function analysis systems?

Innovision ApS’s pulmonary function analysis systems are designed to measure and assess lung function in both adults and children. These systems help clinicians evaluate conditions like asthma, chronic obstructive pulmonary disease (COPD), or other respiratory disorders by quantifying parameters such as airflow, lung volume, and gas exchange efficiency during rest or exercise.

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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Facebook
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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
305276496

Catalogue (13)

DeviceModel / ReferenceRegistriesClassStatus
Innocor INN00500-1a
FDA UDI
Class IIActive
Innocor INN00400-1a
FDA UDI
Class IIActive
Innocor INN00100-1
FDA UDI
Class IIActive
Innocor INN00300-1
FDA UDI
Class IIActive
Innocor INN00500-1c
FDA UDI
Class IIActive
Innocor INN00300
FDA UDI
Class IIActive
Innocor INN00400
FDA UDI
Class IIActive
Innocor INN00500
FDA UDI
Class IIActive
Innocor INN00400-1c
FDA UDI
Class IIActive
Innocor INN00400-1b
FDA UDI
Class IIActive
Innocor INN00100
FDA UDI
Class IIActive
Innocor INN00010-1
FDA UDI
Class IIActive
Innocor INN00010
FDA UDI
Class IIActive

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