Material properties
We check each polymer’s properties and processing methods, then set development specifications for the intended use.
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For healthcare professionals & businesses · No consumer sales
GLOONE / SINCE 2011
GLOONE has researched and processed biodegradable polymers since its founding in 2011. We now operate the Materials, Medical devices and Aesthetics divisions. Material properties, product form and production conditions are reviewed against each client’s target specifications.

Technology gained from processing absorbable plates and screws, as well as polymer filaments, is the basis of our PLLA microsphere development. Even with the same polymer, each application calls for a different form and different manufacturing requirements.
We check each polymer’s properties and processing methods, then set development specifications for the intended use.
We define the structure and dimensions of filaments, particles and molded products, then evaluate them through prototypes.
We align molds, equipment and process conditions to move prototypes into manufacturing.
Materials were analyzed, samples processed, and results examined through testing and observation. Records from different periods show how GLOONE approaches research and development.



Research and manufacturing records from different periods.
Explore research records ↗Materials research, product development, production and quality staff coordinate around the same product specifications. Where development requires it, we seek advice from specialists in the relevant field.
Separate divisions handle material development, medical device manufacturing and aesthetics product planning.
Based at the Eumseong materials site, develops and supplies polymer materials, microspheres, polymer filaments and PCL filament for 3D printing.
MaterialsDevelops and manufactures medical devices, including GLOSORB absorbable plates and screws, and manages quality and supply for each product.
Medical devicesHandles product planning and launch preparation for COG sutures, fillers, skin boosters and cosmetics. Planning draws on development know-how from the Materials division and the OEM/ODM team.
AestheticsThis timeline covers major events from our founding in 2011 to filler and skin booster development.
GLOONE incorporated · 30 September
Dedicated R&D department recognized
Registered as a venture company
Medical-device manufacturing business licence
Medical-device GMP certification
Plate and screw permits · corporate research institute recognized · two PRP-related patents registered
Selected for a Ministry of Science, ICT and Future Planning research project
Selected for a Small and Medium Business Administration research project
Selected for a Ministry of Science, ICT and Future Planning research project
Production of PLLA, PLGA and PCL polymer filaments
Selected as an IP STAR company
Joint venture established in Guangzhou, China
Vietnam authorization for absorbable medical devices
Korean authorization for PP sutures
Joint research on tube and catheter surface coatings
Commissioned development of a PLLA filler
Commissioned research on cosmetics using absorbable materials
Commissioned development of an absorbable fixation device
PLLA filler product development
PLA filter development · plate and screw registration in Vietnam
Wound-dressing and skin-booster development
Meet the researchers who contribute to GLOONE’s work in polymers, materials and processing technology. Explore their expertise and research backgrounds.
These researchers review material properties and processing methods. Affiliations are listed as part of each individual’s background.
KOREATECH · Professor emeritus
Seoul National University, Chemical and Biological Engineering · Professor
University of Ottawa, Cellular and Molecular Medicine · Associate Professor
Hanseo University · Professor
KOREATECH, Energy, Materials and Chemical Engineering · Professor
These profiles describe individual research and advisory participation. They do not imply an institution-wide agreement or any recommendation, use or efficacy endorsement of a specific product.
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MANUFACTURING & QUALITY
Recognized as conforming to Korean medical-device GMP. Supporting documents are available to customers on request.
ISO 13485 certified.
Outline the three points below, and we will review the scope you need, from materials research to processing and manufacturing.
Tell us the material you plan to use and the development problem you want to solve.
List the samples and measurement results you have, and any additional evaluations required.
Let us know the scope of collaboration needed across research, processing and manufacturing, and your preferred timeline.