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Company profile

Smith & Nepew, Inc.

KO: 스미스앤드네퓨(주)
South Korea서울특별시 강남구 영동대로 517 , 13층 일부(삼성동, 아셈타워)737 devicesRegistered Jul 09, 1998 – Feb 02, 2023
VerifiedMFDS · Ministry of Food and Drug Safety registry
737
Total devices
5
Device classes
Jul 09, 1998
Earliest approval
Feb 02, 2023
Latest approval
Regulatory footprint
Search Smith & Nepew, Inc. across other regulatory registries
ThailandEuropean UnionColombiaCanadaEcuadorSaudi Arabia
Device class distribution
Breakdown of 737 devices by regulatory classification
Class I39954.1% of total
Class II11916.1% of total
Unknown10614.4% of total
Class III9713.2% of total
Class IV162.2% of total
Registered devices (10 most recent shown)
Click on any device for detailed registration information
Reusable universal manual medical clamp
재사용가능범용수동식의료용클램프
Feb 02, 2023
Class
Class I
License Number
Reception No. 23-179
Orthopedic calipers
정형외과용캘리퍼스
Feb 01, 2023
Class
Class I
License Number
Reception No. 23-170
Medical Guide
의료용가이드
Jan 19, 2023
Class
Class I
License Number
Reception No. 23-110
Medical Measuring Instrument
의료용측정자
Jan 06, 2023
Class
Class I
License Number
Reception No. 23-40
Medical Measuring Instrument
의료용측정자
Dec 08, 2022
Class
Class I
License Number
Reception No. 22-2102
Osteosplicing staple
골접합용스태플
Nov 22, 2022
Class
Class III
License Number
Suhe 22-258
Artificial hip joint
인공엉덩이관절
Nov 02, 2022
Class
Class III
License Number
Suhe No. 22-235
Invasive Disposable Medical Guide
침습형일회용의료용가이드
Nov 01, 2022
Class
Class II
License Number
Suin 22-4512
Manual bone surgery machine
수동식골수술기
Sep 13, 2022
Class
Class I
License Number
Reception No. 22-1559
Disposable medical suture machine
일회용의료용봉합기
Aug 23, 2022
Class
Class II
License Number
Suin No. 22-4415
View all 737 devices →
About this profile

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.