Quality 2018-11-22T14:26:15+00:00
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History

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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 ) CE Certification and FDA & 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