We are excited to announce that LI Medical Corporation has received U.S. FDA 510(k) clearance (K240434) for our Endometrial Suction Curette, further expanding our line of FDA-cleared OB/GYN diagnostic and surgical instruments.

The Endometrial Suction Curette is a sterile, single-use device designed for efficient and minimally invasive sampling of the endometrial lining. It offers clinicians a safe and effective option for endometrial biopsy and histologic assessment, supporting the early diagnosis and management of gynecologic conditions.

This regulatory clearance underscores our dedication to delivering high-quality, clinically proven solutions that meet the stringent standards of the U.S. healthcare system. Manufactured in our ISO 13485 certified facility with years of OEM expertise, this device is now available under the LI Medical brand, combining reliability, performance, and value.

As we continue to build a comprehensive portfolio of OB/GYN disposables, this achievement reflects our commitment to advancing women’s healthcare and supporting providers with trusted, innovative tools.