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FDA 510(k)

LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer

K-Number: K242830 · 2025-05-30

Decision Date2025-05-30
Product CodePOV
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer is a medical device manufactured by Bonraybio Co., Ltd.. It received FDA 510(k) clearance on 2025-05-30 under approval number K242830. The device is classified under product code POV. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer?

LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer is a medical device that received FDA 510(k) clearance on 2025-05-30. It is manufactured by Bonraybio Co., Ltd.. The 510(k) number is K242830.

When was LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer approved by the FDA?

LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer received FDA 510(k) clearance on 2025-05-30, under approval number K242830.

What company makes LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer?

LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer is manufactured by Bonraybio Co., Ltd..

What is the FDA product code for LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer?

The FDA product code for LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer is POV.

Related Clinical Trials

Other Devices by Bonraybio Co., Ltd.

Related Devices (Code: POV)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.