Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009545293

FEI Number

3009545293

Entity Name

WEIHAI KAIBO MEDICAL DEVICE CO., LTD.

City/State/Country

WEIHAI Shandong, CN

Establishment Address

NO. 9 Fuzhou Rd., Downtown, RUSHAN, WEIHAI Shandong 264500, CN

Establishment Type(s)

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

Owner / Operator

WEIHAI KAIBO MEDICAL DEVICE CO., LTD. (Owner Number: 10040029)

Owner / Operator Contact Address

NO.9 FUZHOU ROAD DOWNTOWN, RUSHAN, WEIHAI, CN-SD 264500, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Hummi Micro Draw Blood Transfer Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KST	System, Blood Collection, Vacuum-Assisted, Manual	Hematology	Class 1	864.9125	2012-03-01

Official Correspondent

Ying Xin

US Agent Details

Scott Olson Business: Kaibo USA Inc Email: s.olson510@yahoo.com Phone: (949) 3008310

Related Public Records

Same Entity

WEIHAI KAIBO MEDICAL DEVICE CO., LTD.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009545293. Last updated year: 2026. Please use registration number 3009545293 when referencing this establishment in official correspondence.