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History

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2-3

2021

2021 Arab Health Exhibition
NAVISEL CE approval
SEEONE VIEW CE approval
SIM-C CE approval
MIXMAX CE approval
BLUEPECKER PLUS CE approval

2020

Selected 2020 export support project
Selected 2020 Overseas standard certification support project
SEEONE VIEW KFDA approval
LIGHT ONE KFDA approval
VIEW ONE KFDA approval
NAVISEL KFDA approval
MIXMAX KFDA approval
SIMC KFDA approval
SW-BMC Kit CE approval
ABMC Kit CE approval
Dotomy CE approval
NTL Bio Gun CE approval

2019

Selected 2019 export support project – Overseas Exhibition support project
Selected 2019 Overseas standard certification support project
LPF 7th Hands-on Interventional Workshop London Exhibition
NASS Exhibition- North American Spine Society
EUROSPINE Exhibition -The Spine Society of Europe
ST.REED PULSE CE approval
CLAUDICARE CE approval
TURTLE GUN CE approval
FORA-B TF CE approval

2018

Selected 2018 export support project – Overseas Exhibition support project
Selected 2018 Overseas standard certification support project
TURTLE GUN KFDA Approval
SW-BMC KIT KFDA Approval
COLEX KFDA   Approval
VEELER PLUS KFDA  Approval
VEELER TF KFDA   Approval
BLUEPEAKER PLUS KFDA  Approval
DOTOMY KFDA   Approval
ABRO CE Certification
FORA-B CE Certification
COLEX CE Certification

2017

Brazil ANVISA approved
FORA-B TF KFDA Approval
Selection Gyeonggi-do Promising Small and Medium Business Capacity Enhancement Project
ST.REED PULSE ( Steerable Pulsed Radio Frequency Catheter System ) KFDA Approval

2016

Selection of 2016 High-Growth enterprise by small & medium business administration
CLAUDICARE ( Percutaneous Endoscopic Neurolysis and ForaminoplastySystem) KFDA Approval

2015

Renewal KGMP and ISO13485
Selection of 2015 High-Growth enterprise by small & medium business administration

2014

Registered as the INNOBIZ
Selection Gyeonggido G-Star
HI-NECK ( Cervical Traction Device )  KFDA Approval
FORA-B ( Steerable Epidural Balloon Catheter System ) and ABRO ( RF Disc Decompression System ) KFDA Approval

2013

ISO9001:2008 & ISO14001:2004 certified by QA international
VEELER ( Vedio Guided Cathter System ) CE Certification and KFDA Approval
HA-DISC ( Heat-Resistance Decompression ) KFDA Approval
SW-PRP ( Autologous Platelet Rich Plasma Kit ) CE Certification

2012

Corporation & Factory transfer to Bucheon
Organization Research Institute recognition
Select as a Promising Small and Medium-sized Enterprise
SW-PRP ( Autologous Platelet Rich Plasma Kit ) KFDA Approval

2011

Registered as the Venture Company by Kibo Technology Fund
ST.REED PLUS ( Steerable epidural catheter system ) CE Certification and KFDA Approval
ST.COX ( Epidural catheter system ) CE Certification and KFDA Approval

2010

2010. 4 Organized Overseas Sales Team
SPASY BCD KIT (Bone Cement Dispensing system) CE Certification and KFDA Approval
ST.REED ( Epidural catheter system ) CE Certification and KFDA Approval

2009

Manufacturing License Issued by KFDA
KGMP Certificate by KFDA
ISO13485:2003 Certified by BSI

2008.11

SEAWON MEDITECH Incorporated by CEO & President Mr.C.Y.Kim
SPASY (kyphoplasty system) CE Certification and KFDA Approval