We approach problems through new structures and perspectives.
NEODOCTOR ABOUT THE COMPANY
VALUE,
ENGINEERED.
Creating value, engineering structure,
and contributing to human health.
CREATIVITY · CHALLENGE · RESPONSIBILITY
02
VISION & MISSION
VISION
Awakening the Body’s
Regenerative Potential.
A global structural-regeneration platform company dedicated to awakening the body's regenerative potentialMISSION
ENGINEERING MECHANICAL INFORMATION FOR TISSUE REGENERATION
We build a medical technology platform that engineers mechanical information through elastic structures.01
WHO WE ARE
FROM MEDICAL DEVICE TO TECHNOLOGY PLATFORM
Building on medical-device technology,
we engineer the environment perceived by tissue.
NeoDoctor researches, develops and manufactures medical devices.
We build a structural regeneration platform connecting material, structure, force and biology.
We turn ideas into verifiable technology.
We grow through quality, evidence and responsibility.
03
CEO MESSAGE
A MEANINGFUL CONTRIBUTION TO MEDICAL SCIENCE
We will create meaningful products
and build value that endures in medicine.
NeoDoctor creates needed products, pursues better technology and shares its value with society.
We study the biological meaning of structure and force and develop shared scientific and clinical standards.
We uphold quality, build evidence and contribute to human health.
CEO, NEO Dr. INC.
04
TECHNOLOGY HERITAGE
FROM VOLUME TO STRUCTURE · FROM STRUCTURE TO CORE
From volume to structure,
from structure to elasticity,
and from elasticity to core.
MULTI THREAD
Explored volume and distribution using multiple filaments
→CAVERN
Designed space and support using a coil-spring structure
→JAMBER
Commercialized a spring structure designed to minimize discomfort
→CORE TECHNOLOGY
Developed elastic-structure technology that stores torsional stress
→JAMBER AI
First product incorporating the core elastic-structure technology
→RE:CORE
An approach to designing tissue structure and its mechanical environment
05
OUR HISTORY
A CONTINUUM OF CREATION
From accumulated manufacturing expertise
to the next medical-technology platform.
MediEnT founded
Company renamed NeoDoctor
MULTI THREAD · Multi-filament structure developed
CAVERN · Coil-spring structure developed
JAMBER · Spring-structure product designed to minimize discomfort
Developed elastic-structure technology that stores torsional stress
JAMBER AI · First product incorporating the core elastic-structure technology developed
RE:CORE · Clinical and educational platform for structural regeneration established
※ This timeline highlights major corporate milestones. Certification status is based on the current information shown in the Quality section below.
06
QUALITY & REGULATORY
EVIDENCE IN EVERY STEP
Trust in technology begins
with a quality system.
We manage quality standards across the full process and market-specific regulatory requirements.
01
QUALITY SYSTEM
Corporate and manufacturing quality foundation
Medical Device Manufacturing License
Republic of Korea Medical Device Manufacturing License No. 2531
Medical Device GMP Certification
Issued 2026.07.07 · Valid through 2029.07.06
Medical Device Quality Management System
EN ISO 13485:2016 · Valid through 2028.12.23
02
PRODUCT & MARKET STATUS
Regulatory status related to PDO absorbable sutures
PDO Absorbable Suture Certification History
Sterile Single Use Absorbable Polydioxanone Suture with Needle · MDD legacy / MDR-transition documentation maintained
PDO Absorbable Suture Registration Approval
Ministry of Health · Approved 2021.11
PDO Absorbable Suture Product Registration
FDA Philippines · Registered 2023.08.30
Medical Device Manufacturing Quality Certification
CBPF · ANVISA · Issued 2024.08.22
03
CORPORATE QUALIFICATIONS
Technology, research and intellectual-property capabilities
Technology-Innovative SME
Valid through 2024.12.28 - 2027.12.27
Management-Innovative SME
Valid through 2024.04.03 - 2027.04.02
Venture Business Certification
Valid through 2024.07.23 - 2027.07.22
Corporate R&D Center Accreditation
Accredited by the Korea Industrial Technology Association
IP Management Certification
Valid through 2021.11.12 - 2029.11.11
DOCUMENT POLICY Because certificates contain controlled information such as identification numbers, addresses and signatures, this website presents current status in text. Official copies are provided to verified partners or upon regulatory request.
REQUEST OFFICIAL DOCUMENTS ↗The scope of certification and registration varies by product and country; the entries shown do not apply uniformly to all JAMBER products. The EU CE entry is based on the available MDD certification history and MDR-transition documentation. Certifications unrelated to JAMBER have been excluded. Current commercial and registration status must be confirmed before contracting or ordering.
42-10 Taejanggongdan-gil, Wonju-si, Gangwon State, Republic of Korea
Rooms 204–205, Building 2, Wonju Medical Device Industry Technology Complex
T. 033-734-1861
E. neodrsales@naver.com
E. jamber@jamber.kr