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Company profile

DIO

KO: (주)디오
South Korea부산광역시 해운대구 센텀서로 66425 devicesRegistered Feb 28, 2003 – Dec 21, 2023
VerifiedMFDS · Ministry of Food and Drug Safety registry
425
Total devices
4
Device classes
Feb 28, 2003
Earliest approval
Dec 21, 2023
Latest approval
Regulatory footprint
Search DIO across other regulatory registries
Device class distribution
Breakdown of 425 devices by regulatory classification
Unknown33578.8% of total
Class I6114.4% of total
Class II194.5% of total
Class III102.4% of total
Registered devices (10 most recent shown)
Click on any device for detailed registration information
About this profile

Complete regulatory portfolio for DIO in South Korea's medical device market. This company has 425 medical devices registered with South Korea MFDS, with registrations dating from Feb 28, 2003 to Dec 21, 2023.

Browse the complete device portfolio including device classifications, license numbers, approval dates, and technical specifications. Pure Global AI provides free access to comprehensive South Korea MFDS registration data, helping global MedTech companies analyze market presence and regulatory compliance for medical device manufacturers in South Korea.