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Asleep Inc

South Korea Last updated 17 Sep 2026

Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

What Asleep Inc makes

Asleep Inc manufactures Sleep Breath Monitoring Software, a digital tool designed to analyze and record respiratory patterns and sleep-related breathing events for diagnostic or monitoring purposes.

The company’s portfolio is classified under EU Medical Device Regulation (MDR) Class I and is registered in the EUDAMED database. The company is based in South Korea.

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

Frequently asked questions

How many devices does Asleep Inc have in the registry?

The registry currently lists 1 device for Asleep Inc. Devices recorded under merged duplicate company entries are counted once.

Which registries list Asleep Inc's devices?

Among its 1 most recently registered device, Asleep Inc has devices listed in EUDAMED (1 device).

What risk classes do Asleep Inc's devices fall under?

Among its 1 most recently registered device, the classes recorded for Asleep Inc's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Asleep Inc in the registry?

The most recently registered devices listed for Asleep Inc include Sleep Breath Monitoring Software.

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

Information

Address
431, Teheran-ro, Gangnam-gu, Seoul, South Korea
Website
asleep.ai
PRRC contact
Sungjin Heo
EUDAMED SRN
KR-MF-000054415