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News in English (USA) / 11.05.2025 / 03:00

FDA Approves First At-Home Cervical Cancer Screening Test, Offering a Pain-Free Alternative to Pap Smears

In a groundbreaking move, the FDA has approved the first at-home cervical cancer screening tool, the Teal Wand™, developed by Teal Health. This innovative device allows women aged 25 to 65, who are at average risk for cervical cancer, to self-collect samples in a comfortable and private setting, potentially replacing the traditional Pap smear. The approval addresses the long-standing discomfort many women experience during gynecological exams and aims to improve screening adherence. Health experts emphasize that while this tool offers convenience, it may not be suitable for everyone and stress the importance of understanding its usage in the broader context of cervical cancer screening.
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