Pure Global

Synex Inc.

(์ฃผ)์‚ฌ์ด๋„ฅ์Šค

Complete regulatory portfolio for Synex Inc. in South Korea's medical device market. This company has 340 medical devices registered with South Korea MFDS, with registrations dating from Sep 15, 1998 to Jan 24, 2024.

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.

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MFDS Official Data
340 Devices
Company Overview
Total Devices
340
Address
์„œ์šธํŠน๋ณ„์‹œ ๊ฐ•๋‚จ๊ตฌ ๋…ผํ˜„๋กœ 430 10์ธต(์—ญ์‚ผ๋™, ์•„์„ธ์•„ํƒ€์›Œ)
Registration Timeline
Earliest Approval
Sep 15, 1998
Latest Approval
Jan 24, 2024
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Device Class Distribution
Breakdown of 340 devices by regulatory classification
Unknown
182
53.5% of total
Class I
77
22.6% of total
Class II
43
12.6% of total
Class III
26
7.6% of total
Class IV
12
3.5% of total
Registered Devices (10 most recent shown)
Click on any device for detailed registration information