Innovision ApS
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Innovision ApS is a medical device manufacturer, with 13 devices listed in FDA GUDID (FDA Class II) as of 13 Nov 2026.
- Devices
- 13
Registry facts
- Registries
- FDA GUDID 13
- Device classes
- FDA Class II 13
- Identifiers
- DUNS 305276496
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.
Catalogue
Search and filter all 13 devicesCompany details
- DUNS number
- 305276496
Frequently asked questions
How many devices does Innovision ApS have in the registry?
The registry currently lists 13 devices for Innovision ApS. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innovision ApS's devices?
Among its 13 most recently registered devices, Innovision ApS has devices listed in FDA GUDID (13 devices).
What risk classes do Innovision ApS's devices fall under?
Among its 13 most recently registered devices, the classes recorded for Innovision ApS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Innovision ApS in the registry?
The most recently registered devices listed for Innovision ApS include Innocor INN00500-1a, Innocor INN00400-1a, Innocor INN00100-1 and Innocor INN00300-1.