DONGGUAN KAISER TECHNOLOGY CO., LTD

FDA Device Registration & Listing · Dongguan city Guangdong, CN · Registration 3009125070

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
3009125070
FEI Number
3009125070
Entity Name
DONGGUAN KAISER TECHNOLOGY CO., LTD
City/State/Country
Dongguan city Guangdong, CN
Establishment Address
No.6, 2nd Road , Sanjiang Industrial Block, Hengli town, Dongguan city Guangdong 523462, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
DONGGUAN KAISER TECHNOLOGY CO., LTD (Owner Number: 10036860)
Owner / Operator Contact Address
No.6, 2nd Road , Sanjiang Industrial Block, Hengli town, Dongguan city, CN-GD 523462, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pulse lavage Upper Face Wrap, Lower Face Wrap, Knee Wrap, Ankle Wrap, Universal Wrap(Small),Elbow Wrap, Hip Wrap, Shoulder Wrap, Universal Wrap(Large),Lumbar Wrap Port Protect Bone Cement Mixer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQH Lavage, Jet General Hospital Class 2 880.5475 2011-06-02
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2023-10-27
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2024-06-05
JDZ Mixer, Cement, For Clinical Use Orthopedic Class 1 888.4210 2013-06-21

Official Correspondent

David Wang

US Agent Details

Jun Vargas Business: Kaiser-Tech inc. LLC Email: jun.kaisermail@gmail.com Phone: (425) 3674018

Related Public Records

Same Entity

DONGGUAN KAISER 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
K213616 Becton, Dickinson and Company BD Surgiphor Antimicrobial Irrigation System 2022-03-23
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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1718850 LivaNova USA, INC. ARVADA, CO, US
3045076544 BEIJING YUEWEI MEDICAL TECHNOLOGY CO., LTD Beijing, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009125070. Last updated year: 2026. Please use registration number 3009125070 when referencing this establishment in official correspondence.
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