CREATION TECHNOLOGIES

FDA Device Registration & Listing · Newark, NY, US · Registration 1000474105

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
1000474105
FEI Number
1000474105
Entity Name
CREATION TECHNOLOGIES
City/State/Country
Newark, NY, US
Establishment Address
328 Silver Hill, Newark, NY 14513, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Creation Technologies (Owner Number: 10042642)
Owner / Operator Contact Address
328 Silver Hill, Newark, NY 14513, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BioWaveGO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2022-05-03

Official Correspondent

Megan Watson

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
2126519 CREATION TECHNOLOGIES WISCONSIN INC. Oak Creek, WI, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K122948 Gemore Technology Co, Ltd. GEM-STIM COMBO STIMULATOR 2012-12-21
K033455 Biomedical Life Systems, Inc. ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5 2004-01-15
K810593 Medical Devices, Inc. NEUROPAC ULTRA I 1981-03-13

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3005170249 Shenzhen Dongdixin Technology Co., Ltd. SHENZHEN Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000474105. Last updated year: 2026. Please use registration number 1000474105 when referencing this establishment in official correspondence.
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