CieloWorks

FDA Device Registration & Listing · Austin, TX, US · Registration 3020696801

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3020696801
FEI Number
3020696801
Entity Name
CieloWorks
City/State/Country
Austin, TX, US
Establishment Address
3724 Executive Center Drive, Suite 205, Austin, TX 78731, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CieloWorks (Owner Number: 10076934)
Owner / Operator Contact Address
3724 Executive Center Drive, Suite 205, Austin, TX 78731, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK200526
PMA Number
N/A

All Registered Proprietary Names

NDDR and CDCS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2021-10-12

Official Correspondent

Dean Goodman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CieloWorks
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 3020696801. Last updated year: 2026. Please use registration number 3020696801 when referencing this establishment in official correspondence.
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