PROTIA INC.
KOSDAQ-listed in-vitro diagnostics company selling PROTIA Allergy-Q allergy diagnostic products domestically and in 80+ countries.
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Business overview
Source: DART corporate disclosureFounded in 2000 and listed on KOSDAQ in 2023, PROTIA is an in-vitro diagnostics medical device company. It sells the PROTIA Allergy-Q human allergy diagnostic line, ANITIA companion-animal allergy tests, food intolerance diagnostics, capacitance-based antibiotic susceptibility tests (Q-AST, PROTIA AST DL001), and autoimmune disease diagnostics. Its allergy diagnostic products hold over 45% domestic market share and reach 80+ countries through roughly 90 distributors, with new products developed under patent acquisition agreements with Yonsei University's industry-academic cooperation foundation.
Products & technology
- PROTIA Allergy-Q serieshuman allergy diagnostics
- ANITIAcompanion animal (dog/cat/horse) allergy diagnostics
- ANITIA Canine Food Intolerance Test 128canine food intolerance diagnostics
- PROTIA AST / Q-AST 192 Proantibiotic susceptibility testing
- IMSAFE Salivasalivary IgA immune antibody measurement
Regulatory approvals
data.go.kr40 Korean MFDS device approvals · 2014–2025
- MFDSIVD reagents for allergy test2025-03-17Product approval · Class 2체외 제인 25-4206 호
- MFDSIVD reagents for allergy test2024-12-30Product approval · Class 2체외 제인 24-1197 호
- MFDSIVD reagents for allergy test2024-12-30Product approval · Class 2체외 제인 24-1196 호
- MFDSIVD reagents for allergy test2024-07-19Product approval · Class 2체외 제인 24-702 호
- MFDSIVD reagents for allergy test2024-07-19Product approval · Class 2체외 제인 24-701 호
- MFDSIVD reagents for allergy test2024-04-26Product approval · Class 2체외 제인 24-441 호
- MFDSMicrobial susceptibility testing analyzer2024-01-29Product approval · Class 1체외 제신 24-131 호
- MFDSIVD reagents for autoimmune disease2023-01-12Product approval · Class 2체외 제인 23-4057 호
- MFDSIVD reagents for infectious disease marker(Diagnosis of Sexually transmitted disease, Legally designated infectious pathogens other than ‘high risk pathogens’, Infectious agents with moderate infectivity), immunological methodRevoked2022-09-29Product approval · Class 3체외 제허 22-651 호
- MFDSIVD reagents for infectious disease marker(Diagnosis of Sexually transmitted disease, Legally designated infectious pathogens other than ‘high risk pathogens’, Infectious agents with moderate infectivity), immunological methodRevoked2022-07-08Product approval · Class 3체외 제허 22-440 호
- MFDSIVD reagents for allergy test2022-06-02Product approval · Class 2체외 제인 22-4425 호
- MFDSIVD reagents for allergy test2022-05-18Product approval · Class 2체외 제인 22-4388 호
Show 28 more
- MFDSIVD reagents and media for antibiotic susceptibility2022-05-18Product approval · Class 2체외 제인 22-4386 호
- MFDSFluorimetric immunoassay analyzer(FIA), stationary2022-04-15Product approval · Class 1체외 제신 22-505 호
- MFDSIVD reagents for infectious disease marker(Diagnosis of Sexually transmitted disease, Legally designated infectious pathogens other than ‘high risk pathogens’, Infectious agents with moderate infectivity), immunological methodRevoked2022-02-09Product approval · Class 3체외 제허 22-84 호
- MFDSMicrobial susceptibility testing analyzerRevoked2021-08-11Product approval · Class 1체외 제신 21-1101 호
- MFDSIVD reagents for infectious disease marker(Diagnosis of Sexually transmitted disease, Legally designated infectious pathogens other than ‘high risk pathogens’, Infectious agents with moderate infectivity), molecular diagnosticsRevoked2021-01-12Product approval · Class 3체외 제허 21-22 호
- MFDSIVD reagents for infectious disease marker(Diagnosis of Sexually transmitted disease, Legally designated infectious pathogens other than ‘high risk pathogens’, Infectious agents with moderate infectivity), molecular diagnosticsRevoked2020-07-15Product approval · Class 3체외 제허 20-570 호
- MFDSIVD reagents for infectious disease marker(Diagnosis of Sexually transmitted disease, Legally designated infectious pathogens other than ‘high risk pathogens’, Infectious agents with moderate infectivity), immunological methodRevoked2020-06-05Product approval · Class 3체외 제허 20-448 호
- MFDSIVD reagents for allergy test2019-12-20Product approval · Class 2체외 제인 19-5034 호
- MFDSIVD reagents for allergy test2019-08-28Product approval · Class 2체외 제인 19-4723 호
- MFDSMicrobial identification analyzer2019-07-18Product approval · Class 1체외 제신 19-996 호
- MFDSIVD reagents and media for antibiotic susceptibility2019-05-23Product approval · Class 2체외 제인 19-4415 호
- MFDSPhotometer for clinical use2019-05-20Product approval · Class 1체외 제신 19-644 호
- MFDSClinical IVD strip for endocrine, related to pregnant2019-04-04Product approval · Class 2체외 제인 19-4257 호
- MFDSBlood sample preparation instruments, general2019-02-22Product approval · Class 1체외 제신 19-244 호
- MFDSMicrobial susceptibility testing analyzer2018-12-14Product approval · Class 1체외 제신 18-1671 호
- MFDSIVD reagents for allergy test2018-08-08Product approval · Class 2체외 제인 18-4635 호
- MFDSImmunoabsorbance analyzer2017-08-25Product approval · Class 1체외 제신 17-990 호
- MFDSIVD reagents for allergy test2017-06-07Product approval · Class 2체외 제인 17-4439 호
- MFDSIVD reagents for allergy test2017-04-06Product approval · Class 2체외 제인 17-4256 호
- MFDSSpectrophotometer for clinical use2017-01-12Product approval · Class 1체외 제신 17-44 호
- MFDSGeneral calibrators, controls or standards, classⅠ, for clinical chemistry2016-04-07Product approval · Class 1체외 제신 16-419 호
- MFDSIVD strip for endocrine self test2016-01-25Product approval · Class 2체외 제인 16-46 호
- MFDSIVD strip for endocrine self test2016-01-25Product approval · Class 2체외 제인 16-47 호
- MFDSChemiluminescence assay(CLIA) analyzer2015-03-18Product approval · Class 1서울 체외 제신 15-100 호
- MFDSSpectrophotometer for clinical use2015-03-10Product approval · Class 1서울 체외 제신 15-89 호
- MFDSIVD reagents for specific protein(immunoglobulin) test2015-03-03Product approval · Class 2체외 제허 15-302 호
- MFDSIVD strip for endocrine self test2014-11-11Product approval · Class 2체외 제인 14-1978 호
- MFDSIVD reagents for allergy test2014-03-18Product approval · Class 2체외 제인 14-644 호
Companies approved for the same productsMedical Devices
Ranked by how many MFDS product categories overlap. Not a ranking — a pointer to where to look.
GC Medical Science Corporation, KOSDAQ-listed since 2014, operates diagnostic reagent, blood glucose, and hemodialysis solution businesses.
Founded in 2011 and KOSDAQ-listed in 2019, Sugentech develops multiplex immunoblot, point-of-care, and digital healthcare diagnostics.
KOSDAQ-listed point-of-care immunodiagnostics company supplying diagnostic cartridges and the ichroma/AFIAS instrument series.
KOSPI-listed in-vitro diagnostics company known for the STANDARD Q antigen/antibody test kits.
Founded in 1987 and listed on KOSDAQ in 2000, NanoenTek develops Lab-On-a-Chip in-vitro diagnostic devices and life science instruments.
Founded 1996, listed on KOSDAQ in 2024, OSANG HEALTHCARE develops and sells biochemistry, immunodiagnostic, and molecular IVD products.
Holds manufacturing approvals for 42 point-of-care diagnostic reagents and devices in the IVD market.
KOSDAQ-listed biotech company developing molecular diagnostics with proprietary C-Tag technology and the NeoPlex product line.
KOSDAQ-listed IVD company producing COVID-19 and HIV point-of-care diagnostic reagents alongside rubber products and entertainment businesses.
KOSDAQ-listed IVD company using SG Cap™ multiplex diagnostic technology for infectious disease, cancer, and companion animal testing.
KOSDAQ-listed IVD company producing time-resolved fluorescence immunodiagnostic products under the Exdia TRF brand.
Established in 2010, listed on KOSDAQ in 2020, QuantaMatrix develops dRAST and QDST antimicrobial susceptibility testing systems.
Sources and updates
- Company basics
- Korea Exchange · DART
- Business content
- Compiled from disclosure filings
- AI visibility
- Measured 2026-08-13
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