CLIP TIP (THAILAND) CO., LTD., the Thailand entity of Clip Tip Co., Ltd., obtained a Medical Device Import Establishment Registration (Registration No. สน. 320/2569) from the Thai Food and Drug Administration (Thai FDA) on August 26, 2026.
The CLIP TIP group is building an integrated platform to support Japanese healthcare and wellness companies entering the Thai market. Our scope extends beyond regulatory support to include local importation, business development, and collaboration with healthcare institutions, key opinion leaders, distributors, and other business partners.
With this registration, CLIP TIP (THAILAND) CO., LTD. has established the required corporate foundation to operate as a medical-device importer in Thailand. Depending on the project, we will be able to design and provide a more integrated pathway spanning Thai FDA application support, importation, storage and logistics, and local partner and channel development.
CLIP TIP (THAILAND) CO., LTD. has already obtained import licenses for cosmetics and hazardous substances. The addition of the medical-device import establishment registration expands the company’s principal import capabilities to three categories:
For food products, we have prepared the internal process needed to promptly pursue the applicable import licenses and authorizations once a concrete project is initiated. For pharmaceutical products, we intend to evaluate and develop the required licensing and import structure on a case-by-case basis, taking into account the product profile and applicable regulatory requirements.
CLIP TIP will continue to combine the following capabilities to support Thai market entry and local commercialization for medical devices, cosmetics, hazardous substances, food products, and other healthcare-related products:
Note: The registration announced here is the Medical Device Import Establishment Registration of CLIP TIP (THAILAND) CO., LTD. It is not a Thai FDA approval or registration for any individual medical device. Actual importation and sale require separate product-level procedures according to the applicable product category, risk classification, and other requirements.