CREATION TECHNOLOGIES WISCONSIN INC.

FDA Device Registration & Listing · Oak Creek, WI, US · Registration 2126519

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
2126519
FEI Number
2126519
Entity Name
CREATION TECHNOLOGIES WISCONSIN INC.
City/State/Country
Oak Creek, WI, US
Establishment Address
2250 W. Southbranch Blvd., Oak Creek, WI 53154, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Creation Technologies (Owner Number: 10045386)
Owner / Operator Contact Address
2250 W. Southbranch Blvd., Oak Creek, WI 53154, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dolphin Jellyfish

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2020-09-21
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2020-09-21
CAF Nebulizer (Direct Patient Interface) Anesthesiology Class 2 868.5630 2020-10-05

Official Correspondent

Raul Federico Pang Villanueva

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Creation Technologies
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004065885 Creation Technologies Everett, WA, US
1000474105 CREATION TECHNOLOGIES Newark, NY, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K163485 Adherium (Nz), Ltd. SmartTouch 2017-08-30
K781467 Travenol Laboratories, S.A. U-FLOAT VALVE 2D9023 1978-09-07

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2126519. Last updated year: 2026. Please use registration number 2126519 when referencing this establishment in official correspondence.
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