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DIMPLO, Ltd.

South KoreaFDA 510(k) applicant, unverified FDA

Devices
522
Registrations
FDA
FDA recalls
0

What DIMPLO, Ltd. makes

DIMPLO, Ltd. manufactures the DIMPLO Implant System, a medical device designed for surgical implantation within the body.

The DIMPLO Implant System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue522

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Company details

DUNS number
963392194

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • DIMPLO Ltd. Yeonje-gu Busan · KR FEI 3042971970