Medical AI Alliance
← Company Index
Biotech & Drug DiscoveryKOSDAQ 04918078 approvals

CELLUMED CO., LTD.

Official website

KOSDAQ-listed holding company making medical devices and biologics including bone graft rhBMP2 and knee implant TKR.

As of 2026-10-09, CELLUMED CO., LTD. has 77 Korean MFDS device approvals, 1 US FDA clearance/approval, 13 PubMed-indexed papers on record (counted by the MAA Company Index from its own matching of public databases).

Price

Change

Market cap

Business overview

Source: DART corporate disclosure

Founded 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 · openFDA

77 Korean MFDS device approvals · 2002–2023 / 1 US FDA 510(k) · 2018

  • MFDSGuide for medical use, invasive, single use2023-09-20
    Product approval · Class 2제인 23-5109 호
  • MFDSGraft, bone, synthetic2022-08-26
    Product approval · Class 4제허 22-582 호
  • MFDSBone graft, animal source or other living things’ source2021-08-10
    Product approval · Class 4제허 21-675 호
  • MFDSClamp, bone, reusableRevoked2021-05-26
    Product approval · Class 1제신 21-767 호
  • MFDSInstruments, bone, surgical, manually-operatedRevoked2021-05-07
    Product approval · Class 1제신 21-625 호
  • MFDSLow frequency electric stimulator for medical use, home useRevoked2021-02-16
    Product approval · Class 2제인 21-4126 호
  • MFDSBone graft, human sourceRevoked2020-10-05
    Product approval · Class 4제허 20-858 호
  • MFDSTissue supplement, collagen2020-06-18
    Product approval · Class 4제허 20-489 호
  • MFDSBone graft material, human sourceRevoked2020-06-01
    Product approval · Class 4제허 20-423 호
  • MFDSInstruments, bone, surgical, manually-operated2020-01-06
    Product approval · Class 1제신 20-22 호
  • MFDSOrthopaedic bone screw, biodegradable2019-10-23
    Product approval · Class 4제허 19-670 호
  • MFDSBone graft material, compositRevoked2019-10-17
    Product approval · Class 4제허 19-655 호
Show 66 more
  • MFDSBone graft material, human sourceRevoked2019-10-17
    Product approval · Class 4제허 19-656 호
  • MFDSGuide for medical use, invasive, single useRevoked2019-10-04
    Product approval · Class 2제인 19-4824 호
  • MFDSBarrier, intra oral, resorbable2019-06-18
    Product approval · Class 4제허 19-374 호
  • MFDSTissue supplement, collagen2018-12-21
    Product approval · Class 4제허 18-823 호
  • MFDSElectrode, external2018-12-12
    Product approval · Class 1제신 18-1645 호
  • MFDSLow frequency electric stimulator for medical use, home use2018-11-09
    Product approval · Class 2제인 18-4928 호
  • MFDSBone graft, composit2018-10-18
    Product approval · Class 4제허 18-688 호
  • MFDSElectrode, external2018-05-08
    Product approval · Class 1제신 18-556 호
  • FDARafugen DBM2018-04-11
    510(k) · TraditionalOrthopedicK180121
  • MFDSOrthopaedic bone screw, biodegradable2017-02-14
    Product approval · Class 4제허 17-108 호
  • MFDSGraft, bone, synthetic2016-11-07
    Product approval · Class 4제허 16-815 호
  • MFDSKnee prosthesis, internal, total biodegradable2015-10-06
    Product approval · Class 4제허 15-1457 호
  • MFDSBone graft material, human source2015-07-03
    Product approval · Class 4제허 15-1076 호
  • MFDSInstruments, bone, surgical, manually-operated2014-05-19
    Product approval · Class 1서울 제신 14-234 호
  • MFDSGuide for medical useRevoked2013-08-27
    Product approval · Class 1서울 수신 13-1810 호
  • MFDSBone graft, human sourceRevoked2013-06-21
    Product approval · Class 4수허 13-1085 호
  • MFDSBone graft, human sourceRevoked2013-06-21
    Product approval · Class 4수허 13-1086 호
  • MFDSBone graft material, human source2013-05-28
    Product approval · Class 4제허 13-922 호
  • MFDSBone graft, human source2013-03-15
    Product approval · Class 4제허 13-550 호
  • MFDSBone graft material, human source2012-12-27
    Product approval · Class 4제허 12-1701 호
  • MFDSGuide for medical use2012-10-11
    Product approval · Class 1서울 제신 12-219 호
  • MFDSBone graft, human source2012-08-24
    Product approval · Class 4제허 12-1087 호
  • MFDSMarker, surgical, externalRevoked2012-04-18
    Product approval · Class 1서울 수신 12-745 호
  • MFDSInjector, medication/vaccine, syringeRevoked2011-12-21
    Product approval · Class 2제허 11-1407 호
  • MFDSGuide for medical useRevoked2011-11-15
    Product approval · Class 1서울 제신 11-242 호
  • MFDSGuide for medical useRevoked2011-11-11
    Product approval · Class 1서울 제신 11-235 호
  • MFDSStereotaxic unit, navigationRevoked2011-10-19
    Product approval · Class 2제인 11-1157 호
  • MFDSHuman cell ＆ Tissue culture incubatorRevoked2011-10-14
    Product approval · Class 1서울 체외 제신 11-209 호
  • MFDSSpinal internal fixation system, intervertebral body2011-06-10
    Product approval · Class 3제허 11-641 호
  • MFDSBone graft, human sourceRevoked2011-05-09
    Product approval · Class 4제허 11-510 호
  • MFDSGuide for medical useRevoked2011-02-25
    Product approval · Class 1서울 제신 11-28 호
  • MFDSInstruments, bone, surgical, manually-operated2011-01-20
    Product approval · Class 1서울 제신 11-8 호
  • MFDSPuncture instrument, surgical, manually-operated, reusableRevoked2011-01-10
    Product approval · Class 1서울 제신 11-5 호
  • MFDSGuide for medical useRevoked2011-01-10
    Product approval · Class 1서울 제신 11-4 호
  • MFDSBone graft material, human sourceRevoked2010-11-23
    Product approval · Class 4제허 10-1232 호
  • MFDSKnee prosthesis, internal, total2010-09-10
    Product approval · Class 3제허 10-916 호
  • MFDSGraft/prosthesis, biomaterial2010-07-27
    Product approval · Class 4제허 10-742 호
  • MFDSGraft/prosthesis, biomaterial2010-07-27
    Product approval · Class 4제허 10-743 호
  • MFDSSpinal internal fixation system, intervertebral bodyRevoked2009-09-16
    Product approval · Class 3제허 09-755 호
  • MFDSSpinal internal fixation system, intervertebral body2009-09-09
    Product approval · Class 3제허 09-723 호
  • MFDS의료용시멘트 분배기Revoked2009-08-25
    Product approval · Class 1서울 제신 09-171 호
  • MFDS의료용천자기(수동식)Revoked2008-12-05
    Product approval · Class 1서울 수신 08-2168 호
  • MFDS의료용천자기(수동식)Revoked2008-09-25
    Product approval · Class 1서울 제신 08-226 호
  • MFDS수술용기구Revoked2008-07-11
    Product approval · Class 1서울 수신 08-1206 호
  • MFDSKnee prosthesis, internal, total biodegradableRevoked2008-03-27
    Product approval · Class 4수허 08-252 호
  • MFDS수술용기구Revoked2007-12-05
    Product approval · Class 1서울 제신 07-295 호
  • MFDS의료용시멘트 분배기Revoked2007-06-08
    Product approval · Class 1서울 제신 07-126 호
  • MFDS골절합용나사Revoked2007-05-20
    Product approval · Class 4수허 07-433 호
  • MFDS의료용클램프(수동식)Revoked2007-04-23
    Product approval · Class 1서울 수신 07-714 호
  • MFDS정형용형판(템플레이트)Revoked2007-04-23
    Product approval · Class 1서울 수신 07-713 호
  • MFDS의료용가이드Revoked2007-04-23
    Product approval · Class 1서울 수신 07-712 호
  • MFDS수술용기구Revoked2007-04-23
    Product approval · Class 1서울 수신 07-711 호
  • MFDSSpinal internal fixation system, intervertebral bodyRevoked2006-05-17
    Product approval · Class 3제허 06-344 호
  • MFDSPuncture instrument, surgical, manually-operated, reusableRevoked2006-04-13
    Product approval · Class 1서울 수신 06-703 호
  • MFDSInstruments, bone, surgical, manually-operatedRevoked2006-04-13
    Product approval · Class 1서울 수신 06-704 호
  • MFDS수술용기구Revoked2006-04-13
    Product approval · Class 1서울 수신 06-705 호
  • MFDSCatheter, infusion, drainageRevoked2004-12-17
    Product approval · Class 2수허 04-1619 호
  • MFDSIrrigation unit, general purpose, manually-operatedRevoked2004-11-05
    Product approval · Class 1경인 수신 04-82 호
  • MFDS골절합용나사Revoked2004-06-29
    Product approval · Class 3수허 04-834 호
  • MFDS수술용기구Revoked2004-04-28
    Product approval · Class 1서울 수신 04-706 호
  • MFDS내시경용삽입유도기구Revoked2004-04-28
    Product approval · Class 1서울 수신 04-707 호
  • MFDS수술용기구Revoked2003-08-28
    Product approval · Class 1서울 수신 03-2424 호
  • MFDS골절합용나사Revoked2003-08-04
    Product approval · Class 3수허 03-930 호
  • MFDS수술용기구Revoked2003-07-29
    Product approval · Class 1서울 수신 03-2140 호
  • MFDSOrthopaedic bone screw, non-biodegradableRevoked2002-04-29
    Product approval · Class 3제허 02-362 호
  • MFDSOrthopaedic bone screw, non-biodegradableRevoked2002-04-29
    Product approval · Class 3제허 02-363 호

R&D and key agreements

Source: DART corporate disclosure

FGF-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

Key disclosures

KRX KIND via OpenDART
Show 34 more events

Publications

PubMed · affiliation-matched
Show 3 more publications

Patents

KIPRIS · applicant-matched
Show 82 more patents

AI reads

MAA server logs · IP-verified
122
Times AI engines pulled CELLUMED CO., LTD.'s records

Pulled records become part of each AI's index and keep feeding its answers. When an AI cites from that index, nothing reaches our server — so actual citations are uncounted here and exceed this number.

1
Fetched fresh mid-answer

Times an AI needed something not yet in its index and fetched this page fresh while answering. Citations served from the index leave no trace here.

121
Index crawls

Collected as raw material for future answers.

0
Direct AI-tool queries (MCP)

Queries from users who connected this index to their own AI.

11
live 0
Last 7 days
90
live 0
Last 30 days
122
live 1
All time
  • OpenAIChatGPT-Userlive1
  • OpenAIOAI-SearchBot98
  • GoogleGoogleOther16
  • PerplexityPerplexityBot3
  • MicrosoftBingbot2
  • AnthropicClaudeBot2

Measured since Aug 27, 2026 · 5 AI engines · last read Oct 9, 2026

User-agent strings can be forged, so we do not count them at face value. We count only requests matched against vendor-published IP ranges, or confirmed by forward-verified reverse DNS. MCP queries are actual calls to this index's tool endpoint.

Connect this index to your AI tool →

Connect this company index directly to your AI

Connect it to ChatGPT or Claude, and your AI queries the full record — profiles, financials, stock data, regulatory approvals, clinical trials, publications and patents — for CELLUMED CO., LTD. and every listed Korean medical, bio and AI company.

How to connect (MCP)
Not yet compiled: business overview. Send us materials and we will add them

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 Co.,Ltd.13 shared

Alpha AI, founded in 1995 and KOSDAQ-listed in 2000, manufactures biocompatible metal implants and surgical instruments.

Corentec Co., Ltd.12 shared

Founded in 2000 and KOSDAQ-listed in 2013, Corentec makes artificial joints; hip and knee implants exceed 85% of revenue.

CG MedTech Co.,Ltd.10 shared

Founded in 1997 and KOSDAQ-listed in 2015, CG MedTech makes orthopedic medical devices and also operates an electric energy business.

MEDYSSEY CO.,LTD10 shared

Manufactures spinal implants and metal 3D-printed patient-specific implants, exporting to over 25 countries.

SHINHUNG CO.,LTD9 shared

Founded in 1964 and KOSPI-listed in 1991, Shinhung manufactures and distributes dental equipment and materials.

OSTEONIC Co., Ltd.9 shared

Established in 2012 and listed on KOSDAQ in 2018, Osteonic manufactures implants for the CMF, Trauma, Sports Medicine, and Spine categories.

HANS BIOMED CORPORATION8 shared

KOSDAQ-listed medical device company producing human tissue implants Bella Cell HD and SureFuse.

JMT CO.,Ltd.8 shared

Provides EMS and SMT manufacturing services for TFT-LCD and OLED panel driver PBAs.

L&K BIOMED CO., LTD.8 shared

Spinal implant device maker founded 2008, listed on KOSDAQ 2016; produces Cervical and Thoraco Lumbar Cage, Screw, and Plate products.

Organ Eco Tech Co.,Ltd.8 shared

Organ Eco Tech, founded in 2006 and KONEX-listed in 2016, manufactures spinal implants.

YUHAN CORPORATION7 shared

Founded in 1926 and listed on the KOSPI in 1962, Yuhan Corporation is a comprehensive pharmaceutical company known for its innovative drug Leclaza.

RootLoc Co., Ltd.5 shared

Founded in 2014 and listed on KONEX in 2020, RootLoc manufactures artificial knee joints and spinal implants for orthopedic surgery.

Sources and updates

Counts on this page are not company-reported figures. MAA matched records from DART, the Korean MFDS, the US FDA, ClinicalTrials.gov, PubMed and KIPRIS to this company itself, by business registration number or registered name, never by name similarity. They may differ from figures the company publishes.

Company basics
Korea Exchange · DART
Business content
Compiled from disclosure filings
Approvals & clinical trials
Korean MFDS (data.go.kr) · US FDA openFDA — updated weekly
Key disclosures
KRX KIND via OpenDART exchange filings — updated daily
Global clinical trials
ClinicalTrials.gov (US NIH) — sponsor-matched, updated weekly
Financials
DART corporate disclosure filings — annual
Publications
PubMed (US National Library of Medicine) — affiliation-matched, updated daily
Patents
KIPRIS (Korea Institute of Patent Information) — applicant-matched, updated monthly
AI reads
Our server logs, IP-verified every 6 hours
AI visibility
Measured 2026-10-01

This page is compiled from public sources without the company's involvement. If anything is inaccurate or incomplete, please let us know. Materials provided by the company are labelled as such.

Request a correction or addition