CELLUMED CO., LTD.
KOSDAQ-listed holding company making medical devices and biologics including bone graft rhBMP2 and knee implant TKR.
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Business overview
Source: DART corporate disclosureFounded in 1985 and listed on KOSDAQ in 2002, CELLUMED is a holding company spanning medical devices, biologics, and cosmeceuticals. It manufactures medical devices such as DBM (demineralized bone matrix) and TKR (knee implants), the growth factor rhBMP-2, and the synovial fluid substitute VISCOSEAL, alongside spinal fixation devices OPS System and CTL System and the FDA-approved EOS Spinal System and Pallas M Spinal System. In 2023, cosmetic ingredient FGF-7 and oral dissolving film (ODF) generated revenue of 535 and 400 respectively (1% share each), and the company is developing an mRNA vaccine production enzyme with a German partner to enter European, Asian, and North American markets.
Products & technology
- TKR (total knee replacement implant)Joint reconstruction implant
- DBM (demineralized bone matrix)Tissue-engineered bone graft material
- rhBMP-2Dental bone graft growth factor
- VISCOSEALSynovial fluid substitute
- FGF-7Skin regeneration cosmetic ingredient / burn treatment ingredient
- ODF (oral dissolving film)Wholesale/retail product
- OPS System / CTL SystemSpinal fixation devices
- EOS Spinal System / Pallas M Spinal SystemSpinal implants
- mRNA vaccine production enzymeEnzyme for mRNA vaccine production
Regulatory approvals
data.go.kr · openFDA77 Korean MFDS device approvals · 2002–2023 / 1 US FDA 510(k) · 2018
- MFDSGuide for medical use, invasive, single use2023-09-20Product approval · Class 2제인 23-5109 호
- MFDSGraft, bone, synthetic2022-08-26Product approval · Class 4제허 22-582 호
- MFDSBone graft, animal source or other living things’ source2021-08-10Product approval · Class 4제허 21-675 호
- MFDSClamp, bone, reusableRevoked2021-05-26Product approval · Class 1제신 21-767 호
- MFDSInstruments, bone, surgical, manually-operatedRevoked2021-05-07Product approval · Class 1제신 21-625 호
- MFDSLow frequency electric stimulator for medical use, home useRevoked2021-02-16Product approval · Class 2제인 21-4126 호
- MFDSBone graft, human sourceRevoked2020-10-05Product approval · Class 4제허 20-858 호
- MFDSTissue supplement, collagen2020-06-18Product approval · Class 4제허 20-489 호
- MFDSBone graft material, human sourceRevoked2020-06-01Product approval · Class 4제허 20-423 호
- MFDSInstruments, bone, surgical, manually-operated2020-01-06Product approval · Class 1제신 20-22 호
- MFDSOrthopaedic bone screw, biodegradable2019-10-23Product approval · Class 4제허 19-670 호
- MFDSBone graft material, compositRevoked2019-10-17Product approval · Class 4제허 19-655 호
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- MFDSBone graft material, human sourceRevoked2019-10-17Product approval · Class 4제허 19-656 호
- MFDSGuide for medical use, invasive, single useRevoked2019-10-04Product approval · Class 2제인 19-4824 호
- MFDSBarrier, intra oral, resorbable2019-06-18Product approval · Class 4제허 19-374 호
- MFDSTissue supplement, collagen2018-12-21Product approval · Class 4제허 18-823 호
- MFDSElectrode, external2018-12-12Product approval · Class 1제신 18-1645 호
- MFDSLow frequency electric stimulator for medical use, home use2018-11-09Product approval · Class 2제인 18-4928 호
- MFDSBone graft, composit2018-10-18Product approval · Class 4제허 18-688 호
- MFDSElectrode, external2018-05-08Product approval · Class 1제신 18-556 호
- FDARafugen DBM2018-04-11
- MFDSOrthopaedic bone screw, biodegradable2017-02-14Product approval · Class 4제허 17-108 호
- MFDSGraft, bone, synthetic2016-11-07Product approval · Class 4제허 16-815 호
- MFDSKnee prosthesis, internal, total biodegradable2015-10-06Product approval · Class 4제허 15-1457 호
- MFDSBone graft material, human source2015-07-03Product approval · Class 4제허 15-1076 호
- MFDSInstruments, bone, surgical, manually-operated2014-05-19Product approval · Class 1서울 제신 14-234 호
- MFDSGuide for medical useRevoked2013-08-27Product approval · Class 1서울 수신 13-1810 호
- MFDSBone graft, human sourceRevoked2013-06-21Product approval · Class 4수허 13-1085 호
- MFDSBone graft, human sourceRevoked2013-06-21Product approval · Class 4수허 13-1086 호
- MFDSBone graft material, human source2013-05-28Product approval · Class 4제허 13-922 호
- MFDSBone graft, human source2013-03-15Product approval · Class 4제허 13-550 호
- MFDSBone graft material, human source2012-12-27Product approval · Class 4제허 12-1701 호
- MFDSGuide for medical use2012-10-11Product approval · Class 1서울 제신 12-219 호
- MFDSBone graft, human source2012-08-24Product approval · Class 4제허 12-1087 호
- MFDSMarker, surgical, externalRevoked2012-04-18Product approval · Class 1서울 수신 12-745 호
- MFDSInjector, medication/vaccine, syringeRevoked2011-12-21Product approval · Class 2제허 11-1407 호
- MFDSGuide for medical useRevoked2011-11-15Product approval · Class 1서울 제신 11-242 호
- MFDSGuide for medical useRevoked2011-11-11Product approval · Class 1서울 제신 11-235 호
- MFDSStereotaxic unit, navigationRevoked2011-10-19Product approval · Class 2제인 11-1157 호
- MFDSHuman cell & Tissue culture incubatorRevoked2011-10-14Product approval · Class 1서울 체외 제신 11-209 호
- MFDSSpinal internal fixation system, intervertebral body2011-06-10Product approval · Class 3제허 11-641 호
- MFDSBone graft, human sourceRevoked2011-05-09Product approval · Class 4제허 11-510 호
- MFDSGuide for medical useRevoked2011-02-25Product approval · Class 1서울 제신 11-28 호
- MFDSInstruments, bone, surgical, manually-operated2011-01-20Product approval · Class 1서울 제신 11-8 호
- MFDSPuncture instrument, surgical, manually-operated, reusableRevoked2011-01-10Product approval · Class 1서울 제신 11-5 호
- MFDSGuide for medical useRevoked2011-01-10Product approval · Class 1서울 제신 11-4 호
- MFDSBone graft material, human sourceRevoked2010-11-23Product approval · Class 4제허 10-1232 호
- MFDSKnee prosthesis, internal, total2010-09-10Product approval · Class 3제허 10-916 호
- MFDSGraft/prosthesis, biomaterial2010-07-27Product approval · Class 4제허 10-742 호
- MFDSGraft/prosthesis, biomaterial2010-07-27Product approval · Class 4제허 10-743 호
- MFDSSpinal internal fixation system, intervertebral bodyRevoked2009-09-16Product approval · Class 3제허 09-755 호
- MFDSSpinal internal fixation system, intervertebral body2009-09-09Product approval · Class 3제허 09-723 호
- MFDS의료용시멘트 분배기Revoked2009-08-25Product approval · Class 1서울 제신 09-171 호
- MFDS의료용천자기(수동식)Revoked2008-12-05Product approval · Class 1서울 수신 08-2168 호
- MFDS의료용천자기(수동식)Revoked2008-09-25Product approval · Class 1서울 제신 08-226 호
- MFDS수술용기구Revoked2008-07-11Product approval · Class 1서울 수신 08-1206 호
- MFDSKnee prosthesis, internal, total biodegradableRevoked2008-03-27Product approval · Class 4수허 08-252 호
- MFDS수술용기구Revoked2007-12-05Product approval · Class 1서울 제신 07-295 호
- MFDS의료용시멘트 분배기Revoked2007-06-08Product approval · Class 1서울 제신 07-126 호
- MFDS골절합용나사Revoked2007-05-20Product approval · Class 4수허 07-433 호
- MFDS의료용클램프(수동식)Revoked2007-04-23Product approval · Class 1서울 수신 07-714 호
- MFDS정형용형판(템플레이트)Revoked2007-04-23Product approval · Class 1서울 수신 07-713 호
- MFDS의료용가이드Revoked2007-04-23Product approval · Class 1서울 수신 07-712 호
- MFDS수술용기구Revoked2007-04-23Product approval · Class 1서울 수신 07-711 호
- MFDSSpinal internal fixation system, intervertebral bodyRevoked2006-05-17Product approval · Class 3제허 06-344 호
- MFDSPuncture instrument, surgical, manually-operated, reusableRevoked2006-04-13Product approval · Class 1서울 수신 06-703 호
- MFDSInstruments, bone, surgical, manually-operatedRevoked2006-04-13Product approval · Class 1서울 수신 06-704 호
- MFDS수술용기구Revoked2006-04-13Product approval · Class 1서울 수신 06-705 호
- MFDSCatheter, infusion, drainageRevoked2004-12-17Product approval · Class 2수허 04-1619 호
- MFDSIrrigation unit, general purpose, manually-operatedRevoked2004-11-05Product approval · Class 1경인 수신 04-82 호
- MFDS골절합용나사Revoked2004-06-29Product approval · Class 3수허 04-834 호
- MFDS수술용기구Revoked2004-04-28Product approval · Class 1서울 수신 04-706 호
- MFDS내시경용삽입유도기구Revoked2004-04-28Product approval · Class 1서울 수신 04-707 호
- MFDS수술용기구Revoked2003-08-28Product approval · Class 1서울 수신 03-2424 호
- MFDS골절합용나사Revoked2003-08-04Product approval · Class 3수허 03-930 호
- MFDS수술용기구Revoked2003-07-29Product approval · Class 1서울 수신 03-2140 호
- MFDSOrthopaedic bone screw, non-biodegradableRevoked2002-04-29Product approval · Class 3제허 02-362 호
- MFDSOrthopaedic bone screw, non-biodegradableRevoked2002-04-29Product approval · Class 3제허 02-363 호
R&D and key agreements
Source: DART corporate disclosureFGF-7 화상치료제 · 화상치료 · 원료 개발중
mRNA 백신 생산효소 · mRNA 백신 생산 공정 · 독일과 위탁개발 진행중 · Aims for overseas contract manufacturing and entry into European, Asian, and North American markets after development
Companies approved for the same productsBiotech & Drug Discovery
Ranked by how many MFDS product categories overlap. Not a ranking — a pointer to where to look.
Alpha AI, founded in 1995 and KOSDAQ-listed in 2000, manufactures biocompatible metal implants and surgical instruments.
Founded in 2000 and KOSDAQ-listed in 2013, Corentec makes artificial joints; hip and knee implants exceed 85% of revenue.
Founded in 1997 and KOSDAQ-listed in 2015, CG MedTech makes orthopedic medical devices and also operates an electric energy business.
Manufactures spinal implants and metal 3D-printed patient-specific implants, exporting to over 25 countries.
Founded in 1964 and KOSPI-listed in 1991, Shinhung manufactures and distributes dental equipment and materials.
Established in 2012 and listed on KOSDAQ in 2018, Osteonic manufactures implants for the CMF, Trauma, Sports Medicine, and Spine categories.
KOSDAQ-listed medical device company producing human tissue implants Bella Cell HD and SureFuse.
Spinal implant device maker founded 2008, listed on KOSDAQ 2016; produces Cervical and Thoraco Lumbar Cage, Screw, and Plate products.
Organ Eco Tech, founded in 2006 and KONEX-listed in 2016, manufactures spinal implants.
Provides EMS and SMT manufacturing services for TFT-LCD and OLED panel driver PBAs.
Founded in 1926 and listed on the KOSPI in 1962, Yuhan Corporation is a comprehensive pharmaceutical company known for its innovative drug Leclaza.
Founded in 2014 and listed on KONEX in 2020, RootLoc manufactures artificial knee joints and spinal implants for orthopedic surgery.
Sources and updates
- Company basics
- Korea Exchange · DART
- Business content
- Compiled from disclosure filings
- AI visibility
- Measured 2026-08-13
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