TAICEND TECHNOLOGY CO., LTD

FDA Device Registration & Listing · Kaohsiung City, TW · Registration 3015172365

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
3015172365
FEI Number
3015172365
Entity Name
TAICEND TECHNOLOGY CO., LTD
City/State/Country
Kaohsiung City, TW
Establishment Address
1F., No 65, Luke 2nd Rd., Luzhu Dist.Kaohsiung City, Taiwan (R.O.C), Kaohsiung City 82151, TW
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TAICEND TECHNOLOGY CO., LTD (Owner Number: 10059435)
Owner / Operator Contact Address
1F., No 65, Luke 2nd Rd., Luzhu Dist.Kaohsiung City, Taiwan (R.O.C), Kaohsiung City, TW-KHH 82151, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TAICEND Medical Adhesive Tape TAICEND PU Film TAICEND Protective Wound Cleansing Mousse TAICEND Liquid Skin Barrier Film TAICEND BB-Barrier Film BB Diaper Spray Baby Wound Protection Mousse TAICEND Medishield Invisible Film TAICEND Scar Care Dressing Scar Care Dressing TAICEND Scar Gel Soothing Hydrogel Nipple Pads

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2022-03-07
NEC Bandage, Liquid, Skin Protectant General Hospital Class 1 880.5090 2019-01-18
MDA Elastomer, Silicone, For Scar Management General, Plastic Surgery Class 1 878.4025 2019-01-18
PFP Silicone Hydrogel For Scar Management General, Plastic Surgery Class 1 878.4025 2024-12-13
NTC Nursing Pad, Hydrogel General Hospital Class 1 880.5630 2021-12-14

Official Correspondent

Yichen Peng

US Agent Details

Catherine Wang Email: cwang90233@gmail.com Phone: (541) 6025889

Related Public Records

Same Entity

TAICEND 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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015172365. Last updated year: 2026. Please use registration number 3015172365 when referencing this establishment in official correspondence.
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