LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SE Semen Quality Analyzer
K-Number: K242830 · 2025-05-30
Device Summary
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.