Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008756262

FEI Number

3008756262

Entity Name

SHENZHEN BESTMAN INSTRUMENT CO.,LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

8th Floor, Yifang Building No.315 Shuangming Avenue, Guangming Street, Guangming District, Shenzhen Guangdong 518107, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen Bestman Instrument CO.,Ltd (Owner Number: 10034759)

Owner / Operator Contact Address

8th Floor, Yifang Building No.315 Shuangming Avenue, Guangming Street, Guangming District, Shenzhen, CN-GD 518107, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K242846

PMA Number

N/A

All Registered Proprietary Names

Models:BF-500B,BF-500+,and BF-500++ Trade/Device name:Doppler fetal heartbeat detector Doppler FHR Detector

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KNG	Monitor, Ultrasonic, Fetal	Obstetrics/Gynecology	Class 2	884.2660	2010-12-29
KNG	Monitor, Ultrasonic, Fetal	Obstetrics/Gynecology	Class 2	884.2660	2025-07-03

Official Correspondent

Yong Bai

US Agent Details

Cancan Huang Business: OSMUNDA TECHNOLOGY CO., LTD. Email: sunny.huang@osmundacn.com Phone: (858) 3571157

Related Public Records

Same Entity

Shenzhen Bestman Instrument 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 3008756262. Last updated year: 2026. Please use registration number 3008756262 when referencing this establishment in official correspondence.