NANCHANG FIRSTOMATO MEDICAL DEVICES CO., LTD.

FDA Device Registration & Listing · Nanchang Jiangxi, CN · Registration 3009208262

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
3009208262
FEI Number
3009208262
Entity Name
NANCHANG FIRSTOMATO MEDICAL DEVICES CO., LTD.
City/State/Country
Nanchang Jiangxi, CN
Establishment Address
No. 555 Aixihu 2 Road, Nanchang Jiangxi 330000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Nanchang Firstomato Medical Devices Co., Ltd. (Owner Number: 10095126)
Owner / Operator Contact Address
No. 555 Aixihu 2 Road, Nanchang, CN-JX 330000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Jewellery, Ear & Nose piercing system, Piercing device and ear hole care solution

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JYS Perforator, Ear-Lobe Ear, Nose, Throat Class 1 874.4420 2026-01-27

Official Correspondent

Ada Zeng

US Agent Details

James St. Wu Business: Humiss Inc. Email: fda-reg@humiss.com Phone: (720) 7595888

Related Public Records

Same Entity

Nanchang Firstomato Medical Devices Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3017517466 KENT-TECH MANUFACTURERS LIMITED HONG KONG, HK
3010892486 DRL Manufacturing S.A. San Pedro de Macoris, DO
3017636737 STERIS Corporation de Republica Dominicana, S.R.L. Santo Domingo, DO
3006749547 RICHLINE GROUP, INC. Tamarac, FL, US
9613926 Gesco Healthcare Private Limited CHENNAI, Tamil Nadu, IN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009208262. Last updated year: 2026. Please use registration number 3009208262 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.