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GYN Surgical Division Likely to Drive Hologic's Q2 Earnings

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Hologic, Inc.’s HOLX  fiscal 2025 second-quarter financial results, set to release on May 1 after the market closes, will likely see a solid performance of its GYN Surgical segment driven by its International strength. Molecular Diagnostics performance is expected to have strongly contributed to the Diagnostics division’s growth. In Breast Health, steady service revenues are expected to have helped offset the capital equipment softness.

Meanwhile, check out our analysis to determine if the stock is worth adding before Q2 earnings.

HOLX’s Segments in Detail

GYN Surgical

We expect the division to be the top performer in the fiscal 2025 second quarter, led by the ongoing strength in its International business, which saw a 20% jump in the previous quarter. Sales of Hologic’s MyoSure and NovaSure devices in Europe likely increased, fueled by the successful execution of its go-direct strategy and an improved reimbursement landscape. Additionally, the U.S. contributions to the related Fluent fluid management system are likely to have aided the growth.

In January 2025, Hologic closed the tuck-in acquisition of Gynesonics into the Surgical portfolio, adding a highly minimally invasive radio frequency ablation tool used to treat uterine fibroids that are less accessible by MyoSure or Accesa. With this addition, sales likely accelerated, leveraging the company’s large GYN sales force, boosting the overall revenue growth in the second quarter.

Our model projects GYN Surgical revenues to increase 3% in the second quarter of fiscal 2025 from the comparable 2024 period.

Diagnostics

The division is expected to have delivered a strong performance in second-quarter fiscal 2025, driven by its core molecular diagnostics business. Ongoing adoption of the BV/CV/TV assay on the Panther platform likely led to this growth, consistent with the past months. Additionally, biotheranostics may have continued to post accretive growth from the expanding use and coverage of the breast cancer index test. Additionally, the respiratory 4-plex, COVID/Flu A/B/RSV assay may have contributed to Diagnsotics’ growth in the second quarter.

Hologic, Inc. Price and EPS Surprise

Hologic, Inc. Price and EPS Surprise
Hologic, Inc. Price and EPS Surprise

Hologic, Inc. price-eps-surprise | Hologic, Inc. Quote

In February 2025, Hologic’s Aptima SARS-CoV-2 assay was granted 510(k) clearance by the FDA, building on its Emergency Use Authorization status in May 2020. Having played a pivotal role in addressing critical testing needs during the pandemic, full FDA clearance likely helped laboratories and clinicians with continued confidence in the test to make informed decisions about patient treatment and healthcare resource management.