WATMIND USA

FDA Device Registration & Listing · Jackson, MS, US · Registration 3021082896

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
3021082896
FEI Number
3021082896
Entity Name
WATMIND USA
City/State/Country
Jackson, MS, US
Establishment Address
4780 I 55 N Ste 450, Jackson, MS 39211, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Watmind USA (Owner Number: 10085767)
Owner / Operator Contact Address
4780 N Frontage Rd., SUITE 450, Jackson, MS 39211, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Speedy Swab Rapid COVID-19 + Flu A&B Antigen Self-Test Speedy Swab Rapid COVID-19 + Flu A&B Antigen Test Speedy Swab Rapid COVID-19 Antigen Self-Test

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QKP Coronavirus Antigen Detection Test System. Unknown Class N N/A 2022-08-03

Official Correspondent

Kyle Rose

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3043128348 Shenzhen Yang Biotech Co., Ltd. Shenzhen Guangdong, CN
3016761091 Shenzhen Watmind Medical Co., Ltd. Shenzhen Guangdong, CN

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2023 Jiangsu Well Biotech Co., Ltd. No N
Jiangsu Well Biotech Co.,Ltd. AND SDI LABS COVID-19 Ag Rapid Test Device - Cat#: CO-02

Similar Registrations

Registration Number Establishment Name Location
3043128348 Shenzhen Yang Biotech Co., Ltd. Shenzhen Guangdong, CN
9610126 ROCHE DIAGNOSTICS GMBH MANNHEIM Baden-Wurttemberg, DE
3008054239 CORE TECHNOLOGY CO., LTD. Changping District Beijing, CN
3016761091 Shenzhen Watmind Medical Co., Ltd. Shenzhen Guangdong, CN
3002642396 Ortho Clinical Diagnostics Singapore South West, SG
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021082896. Last updated year: 2026. Please use registration number 3021082896 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.