SHENZHEN SPONGE NEW MATERIAL CO. LTD

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3043106338

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
3043106338
FEI Number
3043106338
Entity Name
SHENZHEN SPONGE NEW MATERIAL CO. LTD
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
Pingshan Linhui Road,21 Zhongcheng Medical Industry Park,Block A,6/F, Shenzhen Guangdong 518118, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Shenzhen Sponge New Material Co. LTD (Owner Number: 10094571)
Owner / Operator Contact Address
Pingshan Linhui Road,21 Zhongcheng Medical Industry Park,Block A,6/F, Shenzhen, CN-GD 518118, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

(Phyyixs NASAL PLUG)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2025-12-08

Official Correspondent

qun Zhang

US Agent Details

Wilson Li Business: REPF America LLC Email: qagujdsvvt@outlook.com Phone: (719) 2013315

Related Public Records

Same Entity

Shenzhen Sponge New Material Co. LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043106338. Last updated year: 2026. Please use registration number 3043106338 when referencing this establishment in official correspondence.
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