NANJING HI-TECH TAPE PRODUCTS CO. LTD.

FDA Device Registration & Listing · Nanjing Jiangsu, CN · Registration 3014383382

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
3014383382
FEI Number
3014383382
Entity Name
NANJING HI-TECH TAPE PRODUCTS CO. LTD.
City/State/Country
Nanjing Jiangsu, CN
Establishment Address
No.1 Zhushan Road, Gaochun Economic Development Zone, Nanjing Jiangsu 211300, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Nanjing Hi-Tech Tape Products Co. Ltd. (Owner Number: 10057367)
Owner / Operator Contact Address
No.13 GuTan Avenue, GaoChun, Nanjing, CN-JS 211300, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

FIRST AID KIT WITHOUT DRUG OKFLEX cohesive Tapes KIT, SURGICAL INSTRUMENT, DISPOSABLE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OHO First Aid Kit Without Drug General, Plastic Surgery Class 1 878.4014 2021-11-30
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2026-04-15
FQM Bandage, Elastic General Hospital Class 1 880.5075 2018-03-26
KDD Kit, Surgical Instrument, Disposable General, Plastic Surgery Class 1 878.4800 2021-11-30
KTC Bath, Sitz, Nonpowered Physical Medicine Class 1 890.5125 2024-12-02
LJL Detectors And Removers, Lice, (Including Combs) General Hospital Class 1 880.5960 2024-03-29

Official Correspondent

Roger Zheng

US Agent Details

tiande Li Business: HTT Technologies Inc. Email: frank.fang@3hcorp.com Phone: (984) 6662381

Related Public Records

Same Entity

Nanjing Hi-Tech Tape Products Co. Ltd.
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 3014383382. Last updated year: 2026. Please use registration number 3014383382 when referencing this establishment in official correspondence.
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