Lynk Solutec announced the issuance of a GMP (Good Manufacturing Practice) Certificate of Conformity for its LYNKS Frontalis Suspension Set, a suture product used in ptosis correction surgery, on April 24, 2026.

The GMP Certificate of Conformity officially confirms that the product’s manufacturing processes and quality management systems meet international regulatory standards, and represents a key prerequisite for commercial distribution in both domestic and international markets. Following the completion of FDA Class I medical device registration in January 2026, this certification marks another step forward in Lynk Solutec’s regulatory compliance process for the product.

Lynk Solutec plans to leverage this certification to advance distribution partnership discussions and initiate full-scale commercial activities for the product.