Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020207731

FEI Number

3020207731

Entity Name

Sleepiz AG

City/State/Country

Zurich, CH

Establishment Address

Hornbachstrasse 23, Zurich 8008, CH

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Sleepiz AG (Owner Number: 10083842)

Owner / Operator Contact Address

Hornbachstrasse 23, Zurich, CH-ZH 8008, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRZ	Oscillometer	Cardiovascular	Class 2	870.2675	2021-12-25

Official Correspondent

Marta Stepien

US Agent Details

Michelle Lott Email: michelle@leanraqa.com Phone: (520) 2759838

Related Public Records

Same Entity

Sleepiz AG

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020207731. Last updated year: 2026. Please use registration number 3020207731 when referencing this establishment in official correspondence.