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MIS Implants Technologies Ltd.

US

Last updated May 23, 2026

What MIS Implants Technologies Ltd. makes

MIS Implants Technologies Ltd. manufactures dental implant suprastructures, including both permanent and single-use temporary preformed designs. Their portfolio also includes two-piece endosteal dental implants (screw and basket types), reusable surgical procedure kits for dental/maxillofacial procedures, and reusable drill bits for dental fixtures. Additionally, they produce screwing power tool attachments and fluted surgical drill bits for dental applications.

The company’s devices are classified under FDA regulations as Class I and Class II, with products listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does MIS Implants Technologies Ltd. primarily manufacture?

MIS Implants Technologies Ltd. specializes in dental implant-related devices. Their portfolio includes dental implant suprastructures (both permanent and temporary, single-use preformed types), two-piece endosteal dental implants (screw and basket designs), reusable dental/maxillofacial surgical kits, and reusable dental drill bits. They also produce screwing power tool attachments and fluted surgical drill bits for dental applications, focusing on components used in dental restoration and implantology.

Where is MIS Implants Technologies Ltd. based, and how does that affect its regulatory standing?

MIS Implants Technologies Ltd. is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations. The FDA classifies their products as either Class I or Class II, depending on the risk level and intended use, and some of their devices are listed in the FDA’s Unique Device Identifier (UDI) database, which helps track and regulate medical devices in the U.S. market.

Which regulatory registries or databases list MIS Implants Technologies Ltd.’s devices?

MIS Implants Technologies Ltd.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for sale in the United States, ensuring transparency and traceability for healthcare providers and regulators. The inclusion in this database reflects compliance with FDA requirements for device identification and reporting.

How are MIS Implants Technologies Ltd.’s devices classified under FDA regulations?

The FDA categorizes MIS Implants Technologies Ltd.’s devices into Class I or Class II based on their risk levels and intended use. Class I devices generally pose minimal risk and may be exempt from some regulatory controls, while Class II devices require stricter oversight due to moderate risk. For example, reusable surgical kits and drill bits may fall under Class II due to their procedural role in dental surgery, whereas some implant components could be classified as Class I if they present lower risk. The classification determines the regulatory pathway and requirements for authorization.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
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LinkedIn
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Facebook
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Email
—
Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
514576057

Catalogue (2090)

Page 20 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MM-S0330
FDA UDI
Class IIUnknown
MIS Multi Unit MA-N4480
FDA UDI
Class IIActive
Mis CS-HS848
FDA UDI
Class IIActive
Mis MG-IE172
FDA UDI
Class IActive
Mis MH-W0555
FDA UDI
Class IIActive
Mis MK-NIZ6
FDA UDI
Class IIActive
Mis MT-S2413
FDA UDI
Class IActive
Mis MT-BT038
FDA UDI
Class IActive
Mis Mistral MF9-08375
FDA UDI
Class IIActive
Mis CM-WO303
FDA UDI
Class IIActive
Mis MK-0064
FDA UDI
Class IActive
Mis VN-AT103
FDA UDI
Class IIActive
Mis MG-TAS56
FDA UDI
Class IActive
Mis CK-NLC4
FDA UDI
Class IIActive
Mis LC3-00400
FDA UDI
Class IIActive
MIS Locator MB-SZL04
FDA UDI
Class IIUnknown
Mis CS-HS575
FDA UDI
Class IIActive
Mis MT-TP500
FDA UDI
Class IActive
Mis CS-TB001
FDA UDI
Class IIActive
Mis CM-SO173
FDA UDI
Class IIActive
Mis VN-AT001
FDA UDI
Class IIActive
Mis Seven MF7-16420
FDA UDI
Class IIActive
Mis Lance EF5-10500
FDA UDI
Class IIActive
Mis EK-WPK84
FDA UDI
Class IIActive
Mis CN-AN003
FDA UDI
Class IIActive
Mis EH-W5500
FDA UDI
Class IIActive
Mis CK-NIC6
FDA UDI
Class IIUnknown
Mis C1C-11330
FDA UDI
Class IIActive
Mis CK-NPK62
FDA UDI
Class IIActive
Mis MD-RAT01
FDA UDI
Class IIUnknown
Mis VN-TB015
FDA UDI
Class IIActive
Mis MT-RKL21
FDA UDI
Class IUnknown
Mis MG-N1137
FDA UDI
Class IActive
Mis CM-SO302
FDA UDI
Class IIActive
Mis CT-WSI10
FDA UDI
Class IActive
Mis MM-MG450
FDA UDI
Class IIActive
Mis MN-TPA12
FDA UDI
Class IIActive
Mis MW-CPK63
FDA UDI
Class IIUnknown
Mis MW-P0010
FDA UDI
Class IIActive
Mis MK-NPC64
FDA UDI
Class IIActive
Mis MG-LS071
FDA UDI
Class IActive
Mis VN-MAN10
FDA UDI
Class IActive
Mis MN-MAB10
FDA UDI
Class IActive
Mis MA-WC548
FDA UDI
Class IIActive
Mis C1C-10420
FDA UDI
Class IIActive
Mis MH-W4630
FDA UDI
Class IIActive
Mis MM-SP104
FDA UDI
Class IActive
Mis VK-NPK41
FDA UDI
Class IIActive
Mis MM-CE056
FDA UDI
Class IIActive
Mis MW-LOC01
FDA UDI
Class IIActive

Related Companies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • MIS Implants Technologies Ltd. BAR LEV INDUSTRIAL PARK Northern · IL FEI 3004203816