Medical & Healthcare Supplies Manufacturers & Suppliers in Japan

Tokyo, Japan

• Workplace on the state insurance register · gBizINFO

Tokyo, Japan

• Workplace on the state insurance register · gBizINFO
• GMP certificate from a medicines agency · EudraGMDP

Kyoto, Japan

• Applicant to the US FDA for 11 medical devices: Trinias (K252099, 2026-03-24), FDR Visionary Suite (K233719, 2024-03-28), RADspeed Pro (K233722, 2024-02-23) +8. The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510
• Workplace on the state insurance register · gBizINFO

Tokyo, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Applicant to the US FDA for 4 medical devices: Ryurei (K252295, 2026-03-27), DualView Catheter (K250751, 2025-07-17), R2P Radifocus Glidewire Advantage (K240818, 2024-11-26) +1. The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Nagoya, Japan

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 3 medical devices: Tomey Optical Biometer OA-2000 (OA-2000) (K252348, 2025-12-18), Tomey Cornea/Anterior Segment OCT (CASIA2) (K250553, 2025-07-18), EM-4000 Specular Microscope (K171313, 2018-01-19). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Osaka, Japan

• Registered as a manufacturer · Superintendencia de Regulacion Sanitaria de El Salvador

Ashigarakami-Gun Kanagawa, Japan

• Site address listed in a government regulator's register · US FDA device establishment registration
• Registered with the U.S. FDA (active, renewed for the current year)

Musashimurayama Tokyo, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Kyoto, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Odate-shi Akita, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Registered with the market regulator: United States · FDA device establishment registration

Tokyo, Japan

Tokyo, Japan

• Registered as a manufacturer · ALIMS
• ENERGY STAR: Imaging Equipment, CL-E321. · ENERGY STAR certified product database

Ibaraki, Japan

• Registered as a manufacturer · ALIMS
• Registered with the U.S. FDA (active, renewed for the current year)

Tokyo, Japan

• Registered as a manufacturer · ALIMS
• Registered with the U.S. FDA (active, renewed for the current year)

Nagoya, Japan

Osaka, Japan

• Registered as a manufacturer · ALIMS

Tottori, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Shizuoka, Japan

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 1 medical devices: Cumulus Remover (K182002, 2018-10-23). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Tokyo, Japan

Chikuma-shi, Nagano-ken, Japan

• Registered as a manufacturer · ALIMS

Tokyo, Japan

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 12 medical devices: SLIT LAMP SL-D4 (Type: LED) (K262637, 2026-09-18), AUTO KERATO-REFRACTO TONOMETER TRK-3 OMNIA (K253039, 2025-11-07), 3D Optical Coherence Tomography (3D OCT-1(type: Maestro2)) (K233561, 2024-04-10) +9. The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Japan

Gamagori, Japan

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 12 medical devices: Scanning Laser Ophthalmoscope Mirante [SLO/OCT Model] with Image Filing Software NAVIS-EX; Scanning Laser Ophthalmoscope Mirante [SLO Model] with Image Filing Software NAVIS-EX (K221320, 2023-03-30), Ophthalmic Yag Laser System YC-200 (K203130, 2020-12-07), Ophthalmic Yag Laser System YC-200 (K192045, 2019-11-15) +9. The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Kamiina-gun Nagano, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Sabae-shi, Fukui, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Registered with the market regulator: United States · FDA device establishment registration

Kawagoe Saitama, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Registered with the market regulator: United States · FDA device establishment registration

Higashiusuki-gun Miyazaki, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Japan

Hanamaki, Japan

• Registered with the U.S. FDA (active, renewed for the current year)

Japan

Aichi, Japan

• Registered as a manufacturer · ALIMS

Japan

Osaka, Japan

• Workplace on the state insurance register · gBizINFO

Japan

• Registered with the U.S. FDA (active, renewed for the current year)

Iga, Japan

• Registered as a manufacturer · ALIMS

Japan

• Registered as a manufacturer · ALIMS
• Registered with the U.S. FDA (active, renewed for the current year)

Shizuoka, Japan

Saitama, Japan

Tokyo, Japan

• Registered as a manufacturer · Agencia Estatal de Medicamentos y Tecnologias en Salud
• Applicant to the US FDA for 1 medical devices: Synapse 3D, Synapse 3D Base Tools v6.1 (K203103, 2021-02-09). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Hamamatsu, Japan

• Workplace on the state insurance register · gBizINFO
• EAEU product declaration on record, company's role not established · EAEU unified register of certificates and declarations

Kyoto, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Applicant to the US FDA for 1 medical devices: Yumizen C1200, Yumizen C1200 Glucose HK, Sodium Electrode, Potassium Electrode, Chloride Electrode (K183375, 2019-02-12). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Tokyo, Japan

• Workplace on the state insurance register · gBizINFO

Tokyo, Japan

• Registered as a manufacturer · ALIMS
• Workplace on the state insurance register · gBizINFO

Tokyo, Japan

Utsunomiya Tochigi, Japan

• Registered with the U.S. FDA as a Contract Manufacturer
• Site address listed in a government regulator's register · US FDA device establishment registration

Tokyo, Japan

• Listed as a distributor on a manufacturer's own site · TQ Systems USA Inc distributor list
• Workplace on the state insurance register · gBizINFO

Tokyo, Japan

• Workplace on the state insurance register · gBizINFO
• EAEU product declaration on record, company's role not established · EAEU unified register of certificates and declarations

Okazaki, Japan

• Registered with the market regulator: United States · FDA device establishment registration
• Registered with the U.S. FDA (active, renewed for the current year)