PROJECT CU CHALLENGE UNLIMITED

FDA Device Registration & Listing · Saint Louis, MO, US · Registration 3005044959

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
3005044959
FEI Number
3005044959
Entity Name
PROJECT CU CHALLENGE UNLIMITED
City/State/Country
Saint Louis, MO, US
Establishment Address
2828 Brannon Ave, Saint Louis, MO 63139, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Project CU Challenge Unlimited (Owner Number: 10093009)
Owner / Operator Contact Address
2828 Brannon Ave, Saint Louis, MO 63139, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

REVITAL OX DRY SPONGE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQA Scale, Surgical Sponge General Hospital Class 1 880.2740 2025-03-17

Official Correspondent

Jon Edgar

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Project CU Challenge Unlimited
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 3005044959. Last updated year: 2026. Please use registration number 3005044959 when referencing this establishment in official correspondence.
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