Shenzhen Omori Biological Technology Co., Ltd.

FDA Device Registration & Listing · Shenzhen city Guangdong, CN · Registration 3022331717

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
3022331717
FEI Number
3022331717
Entity Name
Shenzhen Omori Biological Technology Co., Ltd.
City/State/Country
Shenzhen city Guangdong, CN
Establishment Address
Floor 4, No.43, LangKou Industrial Park, DaLang Street, LongHua District,, Shenzhen city Guangdong 518109, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
VivaLnk Inc (Owner Number: 10049171)
Owner / Operator Contact Address
51 EAST CAMPBELL AVE., SUITE 160, Campbell, CA 95008, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Temperature Adhesive Disposable Hydrogel Adhesive Fever Scout Adhesive Hydrogel Adhesive VivaLNK Adhesive Patch

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 2018-07-23

Official Correspondent

quoi huynh

US Agent Details

quoi huynh Business: VIVALNK INC Email: qh@vivaLnk.com Phone: (408) 2054202

Related Public Records

Same Entity

VivaLnk Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3017643152 Dongguan CFE Electronic Co., Ltd Dongguan Guangdong, CN
3019737388 Hangzhou VivaLNK Medical Technology Co.,LTD. Hangzhou Zhejiang, CN
3011651103 VIVALNK, INC. Campbell, CA, US

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 3022331717. Last updated year: 2026. Please use registration number 3022331717 when referencing this establishment in official correspondence.
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