XIANTAO XINGRONG PROTECTIVE PRODUCTS CO., LTD.

FDA Device Registration & Listing · Xiantao Hubei, CN · Registration 3007084580

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
3007084580
FEI Number
3007084580
Entity Name
XIANTAO XINGRONG PROTECTIVE PRODUCTS CO., LTD.
City/State/Country
Xiantao Hubei, CN
Establishment Address
Pengchang Ave (South of Xianpeng Road), Xiantao Hubei 433018, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Xiantao Xingrong Protective Products Co., Ltd. (Owner Number: 10057288)
Owner / Operator Contact Address
Pengchang Ave (South of Xianpeng Road), Xiantao, CN-HB 433018, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

COVER SHOE ,OPERATING -ROOM Disposable Mask, Disposable Medical Mask CAP,SURGICAL NON-SURGICAL ,ISOLATION GOWN BEDDING,DISPOSABLE MEDICAL MASK,SCAVENGING

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FXP Cover, Shoe, Operating-Room General, Plastic Surgery Class 1 878.4040 2018-03-15
QKR Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua Unknown Class N N/A 2020-04-11
FYF Cap, Surgical General, Plastic Surgery Class 1 878.4040 2018-03-15
OEA Non-Surgical Gown General, Plastic Surgery Class 1 878.4040 2018-03-15
KME Bedding, Disposable, Medical General Hospital Class 1 880.6060 2018-03-15
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2018-03-15

Official Correspondent

Sabrina Nie

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Xiantao Xingrong Protective Products 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
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06

Similar Registrations

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3013429557 HEYUAN HONG DE MEDICAL PRODUCTS CO., LTD. Heyuan City Guangdong, CN
3038718579 OKETZ LOGISTICS LLC Coral Gables, FL, US
3008808082 PLANET(SHANGHAI) INTERNATIONAL CO.,LTD shanghai, CN
3013823570 GUANGZHOU BAOLI HARDWARE & ELECTRONIC CO.,LTD. Guangzhou Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007084580. Last updated year: 2026. Please use registration number 3007084580 when referencing this establishment in official correspondence.
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