WUXI XINDI MEDICAL TECHNOLOGY CO., LTD

FDA Device Registration & Listing · Wuxi City Jiangsu, CN · Registration 3030234167

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
3030234167
FEI Number
3030234167
Entity Name
WUXI XINDI MEDICAL TECHNOLOGY CO., LTD
City/State/Country
Wuxi City Jiangsu, CN
Establishment Address
No.60, Xinfeng Road, Meicun Town, Xinwu District, Wuxi City Jiangsu 214000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Wuxi XinDi Medical Technology Co., Ltd (Owner Number: 10089348)
Owner / Operator Contact Address
No.60, Xinfeng Road, Meicun Town, Xinwu District, Wuxi City, CN-JS 214000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Silicone scar tape Wound closure device ACNE PATCH, Hydrocolloid patch Adhesive patches Nasal strip

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDA Elastomer, Silicone, For Scar Management General, Plastic Surgery Class 1 878.4025 2023-11-30
FZQ Clip, Removable (Skin) General, Plastic Surgery Class 1 878.4320 2023-11-30
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2024-03-18
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2023-11-30
LWF Dilator, Nasal Ear, Nose, Throat Class 1 874.3900 2023-11-30

Official Correspondent

Yunfei Luo

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Wuxi XinDi Medical Technology Co., Ltd
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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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3009192857 Neodyne Biosciences, Inc. Fremont, CA, US
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3019769561 ScarPro NV Aalter Flanders, BE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030234167. Last updated year: 2026. Please use registration number 3030234167 when referencing this establishment in official correspondence.
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