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Medical DevicesKOSDAQ 38965026 approvals

NEXTBIOMEDICAL Co., Ltd.

Official website

Founded in 2014 and listed on KOSDAQ in 2024, NEXTBIOMEDICAL develops endoscopic hemostats and vascular embolization microspheres.

As of 2026-10-08, NEXTBIOMEDICAL Co., Ltd. has 24 Korean MFDS device approvals, 2 US FDA clearances/approvals, 2 PubMed-indexed papers on record (counted by the MAA Company Index from its own matching of public databases).

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Regulatory approvals

data.go.kr · openFDA

24 Korean MFDS device approvals · 2015–2025 / 2 US FDA 510(k) · 2022–2024

  • MFDSEmbolization implant inserter, intervascular2025-11-19
    Product approval · Class 3제허 25-781 호
  • MFDSEmbolization implant inserter, intervascular2025-07-28
    Product approval · Class 3제허 25-515 호
  • FDANexpowder2024-11-27
    510(k) · TraditionalGeneral, Plastic SurgeryK240994
  • MFDSDressing, absorbable, wound, synthetic polymer2024-11-26
    Product approval · Class 4제허 24-837 호
  • FDANexpowder2022-09-16
    510(k) · TraditionalGeneral, Plastic SurgeryK202929
  • MFDSDressing, absorbable, wound, synthetic polymer2021-12-08
    Product approval · Class 4제허 21-990 호
  • MFDSEmbolization implant inserter, intervascularRevoked2020-12-10
    Product approval · Class 3제허 20-1064 호
  • MFDSStent, duodenalRevoked2020-10-15
    Product approval · Class 3제허 20-887 호
  • MFDSStent, colonRevoked2020-10-15
    Product approval · Class 3제허 20-886 호
  • MFDSEmbolization implant inserter, intervascular2019-06-27
    Product approval · Class 3제허 19-412 호
  • MFDSStent, colonRevoked2018-04-05
    Product approval · Class 3제허 18-229 호
  • MFDSOesophageal stentRevoked2018-04-05
    Product approval · Class 3제허 18-228 호
Show 14 more
  • MFDSStent, duodenalRevoked2018-04-02
    Product approval · Class 3제허 18-216 호
  • MFDSBiliary stentRevoked2018-04-02
    Product approval · Class 3제허 18-215 호
  • MFDSStent, duodenalRevoked2018-03-14
    Product approval · Class 3제허 18-174 호
  • MFDSEndotherapy cannula, single-use2018-02-23
    Product approval · Class 2제인 18-4140 호
  • MFDSDressing, absorbable, wound, synthetic polymer2018-01-09
    Product approval · Class 4제허 18-14 호
  • MFDSStent, colonRevoked2016-07-04
    Product approval · Class 3제허 16-470 호
  • MFDSStent, colonRevoked2016-07-04
    Product approval · Class 3제허 16-469 호
  • MFDSStent, duodenalRevoked2016-06-21
    Product approval · Class 3제허 16-438 호
  • MFDSBiliary stentRevoked2016-02-25
    Product approval · Class 3제허 16-144 호
  • MFDSOesophageal stentRevoked2016-02-18
    Product approval · Class 3제허 16-123 호
  • MFDSENT powder applicatorRevoked2016-02-11
    Product approval · Class 1수신 16-370 호
  • MFDSENT powder applicator2015-11-10
    Product approval · Class 1제신 15-380 호
  • MFDSBiliary stentRevoked2015-11-02
    Product approval · Class 3제허 15-1539 호
  • MFDSOesophageal stentRevoked2015-11-02
    Product approval · Class 3제허 15-1540 호

Key disclosures

KRX KIND via OpenDART

Publications

PubMed · affiliation-matched

Patents

KIPRIS · applicant-matched
Show 31 more patents

AI reads

MAA server logs · IP-verified
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Measured since Aug 27, 2026 · 5 AI engines · last read Oct 7, 2026

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Companies approved for the same productsMedical Devices

Ranked by how many MFDS product categories overlap. Not a ranking — a pointer to where to look.

MITECH CO.,LTD.4 shared

MITECH CO.,LTD., founded in 1991 and listed on KOSDAQ in 2018, makes non-vascular stents and distributes Fujifilm endoscopy equipment.

SEWOONMEDICAL CO,. LTD.3 shared

Founded in 1982 and KOSDAQ-listed in 2008, Sewoon Medical manufactures medical aspirators and catheters/tubes.

BASKHANBIOPharma Inc.1 shared

Founded 1986, KONEX-listed since 2022, BASKHANBIOPharma makes drugs and medical devices for use before and after surgery.

JEIL PHARMACEUTICAL CO.,LTD1 shared

Spun off from Jeil Pharm Holdings in 2017, Jeil Pharmaceutical has licensed out its GERD drug Zastaprazan (Jaqubo) to multiple overseas partners.

INTEROJO CO. LTD.100

Interojo, founded 2000 and KOSDAQ-listed 2010, manufactures contact lenses under its Clalen brand domestically and via OEM/ODM overseas.

JETEMA Co.,Ltd.90

Founded 2009, listed on KOSDAQ in 2019, JETEMA develops hyaluronic acid fillers, botulinum toxin biopharmaceuticals, and lifting threads.

Corentec Co., Ltd.85

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

NanoenTek,Inc.85

Founded in 1987 and listed on KOSDAQ in 2000, NanoenTek develops Lab-On-a-Chip in-vitro diagnostic devices and life science instruments.

SEJONG MEDICAL Co.Ltd.,85

Founded in 2010 and KOSDAQ-listed in 2018, Sejong Medical manufactures laparoscopic surgical instruments.

REMEDI Inc.85

Founded in 2012 and listed on KOSDAQ in 2026, REMEDI develops portable X-ray imaging devices based on its low-dose, miniaturized X-ray technology.

Laseroptek Co., Ltd.85

KOSDAQ-listed medical device company developing the LOTUS and HELIOS laser aesthetic devices and the PALLAS vitiligo treatment device.

AIOBIO Co., Ltd.85

Develops quantitative fluorescence biomarker technology for oral disease diagnostic devices.

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.

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