Dental Supplies & Equipment Manufacturers & Suppliers in South Korea

Goyang-si Gyeonggi, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Registered with the market regulator: United States · FDA device establishment registration

Goyang-si Gyeonggi, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Gunpo-si Gyeonggi, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Daegu, South Korea

• Applicant to the US FDA for 2 medical devices: Multi M Series (K250826, 2025-06-12), DMAX Coloring Liquid; Chang's Liquid; Confident Coloring Liquid; CAMeleon Coloring Liquid (K173769, 2018-03-08). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510
• Site address listed in a government regulator's register · US FDA device establishment registration

Suncheon-si, Jeollanam-do Jeonnam, South Korea

• Site address listed in a government regulator's register · US FDA device establishment registration
• Registered with the U.S. FDA (active, renewed for the current year)

Daegu, South Korea

• Site address listed in a government regulator's register · US FDA device establishment registration
• Registered with the U.S. FDA (active, renewed for the current year)

Uiwang-si, Gyeonggi, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Daejeon, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Applicant to the US FDA for 3 medical devices: SurFuse Gel, SurFuse Putty, ExFuse Gel, ExFuse Putty (K171568, 2018-02-22), MaxiGen (K152077, 2016-04-21), BellaFuse (K151271, 2016-03-11). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Yongin-si Gyeonggi, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Seoul, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Gwangju, South Korea

• Applicant to the US FDA for 2 medical devices: KJ ZIRCONIA Implant System (K173116, 2018-06-28), J2A SLA Dental Implant System (K161923, 2017-11-09). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510
• Site address listed in a government regulator's register · US FDA device establishment registration

Seoul, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Jincheon-gun Chungbuk, South Korea

• Registered as a manufacturer · ALIMS
• Site address listed in a government regulator's register · US FDA device establishment registration

Goyang-si Gyeonggi, South Korea

• Registered as a manufacturer · ALIMS
• Site address listed in a government regulator's register · US FDA device establishment registration

Saha-gu Busan, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Heungdeok-gu Cheongju-si Chungbuk, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Gun Po Si Gyeonggi, South Korea

• Registered with the U.S. FDA as a Contract Manufacturer
• Registered with the market regulator: United States · FDA device establishment registration

Seoul, South Korea

• Applicant to the US FDA for 2 medical devices: K3 (K183347, 2019-09-04), K3 (K152830, 2017-04-20). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510
• Registered with the U.S. FDA (active, renewed for the current year)