CLARITY DESIGN, INC.

FDA Device Registration & Listing · Poway, CA, US · Registration 3011883032

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
3011883032
FEI Number
3011883032
Entity Name
CLARITY DESIGN, INC.
City/State/Country
Poway, CA, US
Establishment Address
13000 Gregg Street, Suite B, Poway, CA 92064, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Clarity Design Inc (Owner Number: 10049915)
Owner / Operator Contact Address
13000 Gregg Street, Suite B, Poway, CA 92064, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Nubody Skin Toning Device

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes Neurology Class 2 882.5890 2018-01-03
MWJ Electrocardiograph, Ambulatory (Without Analysis) Cardiovascular Class 2 870.2800 2025-12-31
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes Neurology Class 2 882.5890 2024-12-30

Official Correspondent

Thomas Lupfer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Clarity Design Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3010872290 Biosonic Technologies, LLC Las Vegas, NV, US
3029083714 The Beauty Tech Group LLC Pleasant Hill, CA, US
3017133271 ROSTI INTEGRATED MANUFACTURING SOLUTIONS (SUZHOU) CO., LTD. Suzhou Jiangsu, CN
3001236514 NSE PRODUCTS, INC. Provo, UT, US
3017953405 SHENZHEN HUAYAN E-COMMERCE CO., LTD. Shenzhen Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011883032. Last updated year: 2026. Please use registration number 3011883032 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.