Pure Global

Smith & Nepew, Inc.

์Šค๋ฏธ์Šค์•ค๋“œ๋„คํ“จ(์ฃผ)

Complete regulatory portfolio for Smith & Nepew, Inc. in South Korea's medical device market. This company has 737 medical devices registered with South Korea MFDS, with registrations dating from Jul 09, 1998 to Feb 02, 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.

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MFDS Official Data
737 Devices
Company Overview
Total Devices
737
Address
์„œ์šธํŠน๋ณ„์‹œ ๊ฐ•๋‚จ๊ตฌ ์˜๋™๋Œ€๋กœ 517 , 13์ธต ์ผ๋ถ€(์‚ผ์„ฑ๋™, ์•„์…ˆํƒ€์›Œ)
Registration Timeline
Earliest Approval
Jul 09, 1998
Latest Approval
Feb 02, 2023
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Device Class Distribution
Breakdown of 737 devices by regulatory classification
Class I
399
54.1% of total
Class II
119
16.1% of total
Unknown
106
14.4% of total
Class III
97
13.2% of total
Class IV
16
2.2% of total