ANSION TECHNOLOGY LIMITED

FDA Device Registration & Listing · SHEUNG WANHONG KONG, HK · Registration 3033530430

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
3033530430
FEI Number
3033530430
Entity Name
ANSION TECHNOLOGY LIMITED
City/State/Country
SHEUNG WANHONG KONG, HK
Establishment Address
FLAT/RM B3, 19/F.TUNG LEECOMMERCIAL BUILDING, 91-97JERVOIS STREET, SHEUNG WANHONG KONG 999077, HK
Establishment Type(s)
Repack or Relabel Medical Device,Foreign Private Label Distributor
Owner / Operator
ANSION TECHNOLOGY LIMITED (Owner Number: 10091959)
Owner / Operator Contact Address
FLAT/RM B3, 19/F.TUNG LEECOMMERCIAL BUILDING, 91-97JERVOIS STREET, SHEUNG WANHONG KONG, HK-NOTA 999077, HK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Fullot, H-Shaped Shower Chair, model MS1421 Fullot, H-Shaped Shower Chair, model MS1121 Fullot, Triangle Shower Chair, model MS1141 FULLOT, Square Shower Chair with Back and Arms, model MS3131, MS3431 Fullot, Triangle Shower Chair, model MS1441 Fullot, H-Shaped Shower Chair with Back and Arms, model MS3121, MS3421 Duppa, Cervical Neck Pillow, model NT1313 Duppa, Neck Brace, model NB4816 DUPPA, Dual Support Sleep Pillow, model NP4517

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILS Adaptor, Hygiene Physical Medicine Class 1 890.5050 2024-11-20
IQK Orthosis, Cervical Physical Medicine Class 1 890.3490 2024-11-20

Official Correspondent

Yoyo Yang

US Agent Details

Hui Hong Business: ABMED MEDICAL TECHNOLOGY INC Email: info@abmed.us Phone: (303) 8000162

Related Public Records

Same Entity

ANSION TECHNOLOGY LIMITED
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K830425 Maddak, Inc. TOILET SEAT RAISED 1983-05-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0006-2025 Ossur H F Grjothals 5 Reykjavik Iceland 1
Miami J Select Collar, Catalog: MJS-101; Miami J Select Collar Set, Catalog: MJSR-101

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033530430. Last updated year: 2026. Please use registration number 3033530430 when referencing this establishment in official correspondence.
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