Shenzhen Boomingshing Medical Device Co., Ltd

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3006795808

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
3006795808
FEI Number
3006795808
Entity Name
Shenzhen Boomingshing Medical Device Co., Ltd
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
3 Yeda Road, Shahu Community, Biling Street, RM 101, Bldg 2, Pingshan District, Shenzhen Guangdong 518118, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Shenzhen BoomingShing Medical Equipment Co., Ltd (Owner Number: 10023017)
Owner / Operator Contact Address
3 Yeda Road, Shahu Community, Biling Street RM 101, Bldg 2, Pingshang District, 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

Pasteur pipettes Inoculation Loops; Inoculation Need Co-Filter Tip, Assay Tip/ AssayCup Tray (E2G) cobas omni Amplication Plate 24 LightCycler 480 Multiwell Plate 384,1 barcode, LightCycler 480 Multiwell Plate 384, 4 bar codes cobas omni Processing Plate, MagNA Pure 96 Processing Cartridge, MagNA Pure 96 Output Plate, cobas omni Pipet te Tips EmbryoSlide+culture dish SURGICAL APPAREL, procedure face mask Labware, assisted Reproduction Culture Dish 40mm, 5 Well Culture Dish, ICSI Dish, Centre Well Dish, Micro-droplet Culture Dish Culture Dish assisted reproduction

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQK Labware, Assisted Reproduction Obstetrics/Gynecology Class 2 884.6160 2021-01-15
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use Clinical Chemistry Class 1 862.2050 2008-02-29
MQK Labware, Assisted Reproduction Obstetrics/Gynecology Class 2 884.6160 2022-02-08
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2020-03-11
PUD Labware, Assisted Reproduction, Exempt Obstetrics/Gynecology Class 2 884.6160 2019-12-24
MQK Labware, Assisted Reproduction Obstetrics/Gynecology Class 2 884.6160 2019-12-24

Official Correspondent

Huanchang Li

US Agent Details

Lisa Liu Business: BioMed Resource Inc. Email: lisal@bmres.com Phone: (310) 3233888

Related Public Records

Same Entity

Shenzhen BoomingShing Medical Equipment Co., Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2008 Beckman Coulter Inc 1
FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013 Biomerieux Inc 1
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006795808. Last updated year: 2026. Please use registration number 3006795808 when referencing this establishment in official correspondence.
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