Booguu Company Limited

FDA Device Registration & Listing · Pak Shek Kok, N.T., HK · Registration 3030656808

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
3030656808
FEI Number
3030656808
Entity Name
Booguu Company Limited
City/State/Country
Pak Shek Kok, N.T., HK
Establishment Address
Unit 225A, 2/F, Core Building 2, 1 Science Park West Avenue,, Hong Kong Science Park,, Pak Shek Kok, N.T. 0000, HK
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Booguu Company Limited (Owner Number: 10090262)
Owner / Operator Contact Address
Unit 225A, 2/F, Core Building 2, 1 Science Park West Avenue, Hong Kong Science Park, Pak Shek Kok, N.T., HK-NOTA 0000, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Aspire Motion Aspire Motion Connect Aspire Motion Pro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISD Exerciser, Measuring Physical Medicine Class 2 890.5360 2024-03-07

Official Correspondent

Gary Jin

US Agent Details

Gary Jin Business: Surge Motion Inc. Email: gary.jin@surgemotion.bio Phone: (503) 8774838

Related Public Records

Same Entity

Booguu Company Limited
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 3030656808. Last updated year: 2026. Please use registration number 3030656808 when referencing this establishment in official correspondence.
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