Medical & Healthcare Supplies Manufacturers & Suppliers in Israel

Modi’in, Israel

• Site address listed in a government regulator's register · Israel Ministry of Environmental Protection

Caesarea, Israel

• Applicant to the US FDA for 4 medical devices: XSense Cryoablation System with CryoProbes (K260377, 2026), ProSense™ System (DEN220077, 2025), XSense Cryoablation System with Cryoprobes (K240892, 2024) +1. The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510
• Registered with the U.S. FDA (active, renewed for the current year)

Yokneam, Israel

• Applicant to the US FDA for 8 medical devices: DEFINE System (AG612444A) (K242598, 2024), InMode Multi-system (K221571, 2022), Evolve System with the T3 Applicator (K210877, 2021) +5. The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510
• Registered with the U.S. FDA (active, renewed for the current year)

Haifa, Israel

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

Rehovot, Israel

Yavne, Israel

Rehovot, Israel

Lod, Israel

Haifa, Israel

Holon, Israel

Afula, Israel

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 3 medical devices: Adin Long Dental Implant System (K252031, 2026), Adin Customized Abutments (K250178, 2025), UniFit Dental Implant System (K223714, 2023). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Tel Aviv, Israel

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 8 medical devices: BriefCase-Triage (K261317, 2026), BriefCase-Triage: CARE Multi-Triage CT for Pneumothorax; Pericardial effusion; Large aortic aneurysm; Shoulder fracture or dislocation device (K253578, 2026), BriefCase (K213886, 2022) +5. The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Modi'in, Israel

• Registered as a manufacturer · ALIMS

Rehovot, Israel

• Registered as a manufacturer · ALIMS

Misgav, Israel

• Registered as a manufacturer · ALIMS

Kiryat Bialik, Israel

• Registered as a manufacturer · Agencia Estatal de Medicamentos y Tecnologias en Salud

Tel-Aviv-Yafo, Israel

• Registered as a manufacturer · ALIMS

Yavne, Israel

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 1 medical devices: BiliWrap (K243372, 2025). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Raanana, Israel

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

Kefar Sava, Israel

• Registered as a manufacturer · ALIMS

Jerusalem, Israel

• Registered as a manufacturer · ALIMS
• Site address listed in a government regulator's register · US FDA device establishment registration

Tel Aviv, Israel

• Registered as a manufacturer · Agencia Estatal de Medicamentos y Tecnologias en Salud

Raanana, Israel

• Registered as a manufacturer · ALIMS

Netanya, Israel

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 3 medical devices: Tixel i (TXLI0001) (K240512, 2024), Tixel® 2 System (K223033, 2023), Tixel System (K202988, 2021). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Tirat HaCarmel, Israel

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

Petah Tikva, Israel

• Registered as a manufacturer · ALIMS

Caesarea, Israel

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 6 medical devices: VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464) (K254001, 2026), TruSPECT Processing Station (K253532, 2025), VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464) (K230600, 2023) +3. The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Tel Aviv, Israel

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 2 medical devices: VIOLA (K230248, 2023), VIOLA (K203307, 2021). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Ra’anana, Israel

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

Rosh Ha'Ayin, Israel

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 2 medical devices: NIO+ Adult (K211968, 2021), NIO-P (K160805, 2016). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Holon, Israel

Haifa, Israel

• Registered as a manufacturer · Superintendencia de Regulacion Sanitaria de El Salvador
• Site address listed in a government regulator's register · Israel Ministry of Environmental Protection

Tel Aviv, Israel

• Medicines manufacturing or import authorisation (MIA) · EudraGMDP manufacturing and importation authorisation register
• Site address listed in a government regulator's register · Israel Ministry of Environmental Protection

Jerusalem, Israel

Israel

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

Beit She'An, Israel

Israel

• Registered as a manufacturer · ALIMS

Yoqneam, Israel

• Applicant to the US FDA for 1 medical devices: LITEDUO (K073411, 2008). The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510
• Registered with the U.S. FDA (active, renewed for the current year)

Israel

Israel

Israel

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

Israel

• Registered as a manufacturer · ALIMS
• Applicant to the US FDA for 8 medical devices: LONGY Implant and LONGY-N Implant (K241462, 2025), Conical Platform Dental Implants System (K240202, 2024), Noris Medical Dental Implants System - Cortical (K210852, 2022) +5. The applicant answers for the notification; the record does not say who makes the device · FDA premarket notifications 510

Israel

Israel

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

Israel

Israel

TEFEN Northern, Israel

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

Bnei Brak, Israel