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LEPU ScienTech Medical Technology (2291) H2 2023 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for LEPU ScienTech Medical Technology (Shanghai) Co Ltd

H2 2023 earnings summary

16 Oct, 2026

Executive summary

  • FY2023 revenue rose 31.6% YoY to RMB325.9m; net profit attributable to owners was RMB151.5m versus a RMB19.8m loss in FY2022, and adjusted net profit increased 55.4% to RMB172.6m.

  • Operating cash flow rose 150.7% YoY to RMB164.3m; year-end assets were RMB1,986.5m and net assets RMB1,926.7m.

  • Growth was led by congenital heart disease occluders and rapid commercialization of biodegradable PFO occluders; the portfolio included 22 marketed products, 9 in registration stages and 24 R&D candidates.

Financial highlights

  • Revenue increased 31.6% to RMB325.9m; gross profit rose 31.5% to RMB288.8m, with gross margin broadly stable at 88.6% versus 88.7%.

  • Operating profit was RMB158.7m versus an operating loss in FY2022; profit before tax was RMB173.3m versus a RMB15.0m loss, and net profit was RMB151.5m versus a RMB19.8m loss.

  • R&D expenses increased 14.3% to RMB61.6m; distribution expenses rose 29.6% to RMB50.1m, while G&A expenses fell 20.2% to RMB42.8m, mainly on lower listing expenses.

  • Net other income was RMB18.4m versus net other losses of RMB69.5m in FY2022; net finance income was RMB14.6m versus net finance costs of RMB13.3m.

  • Basic and diluted EPS was RMB0.44 versus a loss of RMB0.06; income tax expense increased to RMB21.8m from RMB4.8m as taxable profit rose.

Outlook and guidance

  • MemoSorb biodegradable ASD occluder approval and commercialization were expected in Q2 2024; ScienCrown TAVR marketing approval was expected in Q4 2024, subject to NMPA review.

  • Atrial septal radiofrequency puncture approval was expected in H1 2024; transapical mitral valve clip registration filing was planned for H1 2024.

  • Aortic valve catheter accessory approval was expected in H2 2024; super stiff guidewire approval was expected by year-end 2024, following a planned Q2 registration submission.

  • Clinical trials for the aortic regurgitation valve candidate were planned for 2025; strategy prioritizes biodegradable technology, product development, domestic market expansion and overseas channels.

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