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Capsule Technologie

Also registered as Capsule Technologie Sas

Country not established

Devices
9

What Capsule Technologie makes

Capsule Technologie manufactures patient monitoring systems, including the SmartLinx Vitals Plus for real-time vital sign tracking, and modifications to the DATACAPTOR device, which appears to support data capture and transmission in clinical settings.

The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

How many devices does Capsule Technologie have in the registry?

The registry currently lists 9 devices for Capsule Technologie. Devices recorded under merged duplicate company entries are counted once.

Which registries list Capsule Technologie's devices?

Among its 9 most recently registered devices, Capsule Technologie has devices listed in FDA 510(k) (9 devices).

What risk classes do Capsule Technologie's devices fall under?

Among its 9 most recently registered devices, the classes recorded for Capsule Technologie's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Capsule Technologie in the registry?

The most recently registered devices listed for Capsule Technologie include SmartLinx Vitals Plus NIBP Module, SmartLinx Vitals Plus License for Spot Monitoring Mode, SmartLinx Vitals Plus Alarm Hub, SmartLinx Vitals Plus License for Advanced Monitoring Mode, Covidien FILAC 3000 - Temperature Module, MODIFICATION TO DATACAPTOR, Capsule Vitals Plus Patient Monitoring System and SmartLinx Vitals Plus Patient Monitoring System.

Generated automatically from registry data and not verified by a human reviewer.