510(k) K242830

Device
LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer
Applicant
Bonraybio Co., Ltd.
510(k) number
K242830
Product code
POV
Decision
Substantially Equivalent (SESE)
Decision date
2025-05-30
Date received
2024-09-19
Regulation
864.5220
Classification name
Semen Analysis Device
Medical specialty
Hematology
Review panel
Hematology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Clare Huang
Address
4f., # 118, Gongye 9th Rd., Dali Dist. Taichung TW 41280 41280

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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K242388LensHooke X12 PRO Semen Analysis SystemBonraybio Co., Ltd.2025-05-09
K243114SQA-iOw Sperm Quality AnalyzerMedical Electronic Systems , Ltd.2025-05-02
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K172514Trak Plus Male Fertility Testing SystemSandstone Diagnostics, Inc.2017-11-17
K161493YO Home Sperm TestMedical Electronic Systems , Ltd.2016-11-08
K153683Trak Male Fertility Testing SystemSandstone Diagnostics, Inc.2016-05-16
K100341SPERMCHECK FERTILITYPrinceton BioMeditech Corp.2010-05-04
K073039SPERMCHECK VASECTOMYPrinceton BioMeditech Corp.2008-01-24
K071737GENERAL SEMEN ANALYSIS KITDyn-Bioshaf (2006) , Ltd.2007-10-25
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