Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030528528

FEI Number

3030528528

Entity Name

NINGBO BETTERLIFE LIMITED

City/State/Country

NINGBO Zhejiang, CN

Establishment Address

820, BUILDING 1, NORTH DISTRICT, QIYUN, 86 MICRO FILM INDUSTRIAL PARK, NO.86, QIYUN ROAD, HAISHU DISTRICT, NINGBO Zhejiang 315000, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

NINGBO BETTERLIFE LIMITED (Owner Number: 10094971)

Owner / Operator Contact Address

820, BUILDING 1, NORTH DISTRICT, QIYUN, 86 MICRO FILM INDUSTRIAL PARK, NO.86, QIYUN ROAD, HAISHU DISTRICT, NINGBO, CN-ZJ 315000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Elastic Bandage Wrap Pimple Patches, COMPRESSED TOWELS Cotton Ball Waterproof Adhesive Bandages, Waterproof Foam Tape/Moleskin Padding Roll Wet Tissue

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2026-01-11
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2026-01-11
EFN	Cotton, Roll	Dental	Class 1	872.6050	2026-01-11
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2026-01-11
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2026-01-11

Official Correspondent

XIAOJUN KONG

US Agent Details

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

Related Public Records

Same Entity

NINGBO BETTERLIFE LIMITED

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
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

Similar Registrations

Registration Number	Establishment Name	Location
3005423373	TRI-FI KNITTING, LLC	Dunlap, TN, US
3008973900	SAFECARE MEDICAL PRODUCTS CO., LTD. (HEFEI)	HEFEI Anhui, CN
3005360866	QEL DOMINICANA S.A.	ESPERANZA Valverde, DO
3015414796	COMPRESS INNOVATIONS, LLC	Manhasset, NY, US
3004651767	CLEARPOINT MEDICAL	Lachine Quebec, CA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030528528. Last updated year: 2026. Please use registration number 3030528528 when referencing this establishment in official correspondence.