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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 18 of 42
DeviceModel / ReferenceRegistriesClassStatus
MIS Multi Unit CM-N4480
FDA UDI
Class IIActive
Mis CW-IT300
FDA UDI
Class IActive
Mis MT-P2411
FDA UDI
Class IUnknown
Mis MG-N1633
FDA UDI
Class IActive
MIS Equator CK-SOE1
FDA UDI
Class IIActive
Mis Lance EF5-08375
FDA UDI
Class IIActive
Mis V3C-10500
FDA UDI
Class IIActive
Mis MK-NPC63
FDA UDI
Class IIActive
Mis V3-11430
FDA UDI
Class IIActive
Mis MT-RI050
FDA UDI
Class IUnknown
Mis MD-AT252
FDA UDI
Class IIActive
Mis MD-TC033
FDA UDI
Class IIActive
Mis CT-NSM30
FDA UDI
Class IActive
Mis MK-CDS13
FDA UDI
Class IActive
Mis CT-SSR30
FDA UDI
Class IActive
Mis CS-MAN10
FDA UDI
Class IActive
Mis MF7-D16420
FDA UDI
Class IIActive
Mis MT-MUML2
FDA UDI
Class IActive
Mis MT-S3508
FDA UDI
Class IActive
Mis Mistral MF9-13375
FDA UDI
Class IIActive
Mis MH-W0655
FDA UDI
Class IIActive
Mis CG-D1039
FDA UDI
Class IActive
Mis MW-P1510
FDA UDI
Class IIActive
Mis VN-TCI23
FDA UDI
Class IIActive
Mis CM-NO302
FDA UDI
Class IIActive
Mis C1 C1-10330
FDA UDI
Class IIActive
Mis CG-NTAS1
FDA UDI
Class IActive
Mis VS-HS858
FDA UDI
Class IIActive
Mis MF7-18420
FDA UDI
Class IIActive
Mis CN-IN360
FDA UDI
Class IIActive
MIS Locator MB-NZL00
FDA UDI
Class IIUnknown
Mis MW-TPA12
FDA UDI
Class IIActive
MIS Equator CK-WOE3
FDA UDI
Class IIActive
Mis CM-SO303
FDA UDI
Class IIActive
Mis C1 C1-11375
FDA UDI
Class IIActive
Mis CF5-08375
FDA UDI
Class IIActive
Mis MH-A5375
FDA UDI
Class IIActive
Mis ED-WMAC1
FDA UDI
Class IIUnknown
Mis MW-IT100
FDA UDI
Class IActive
Mis LT-SSM10
FDA UDI
Class IActive
Mis MN-AN020
FDA UDI
Class IIActive
Mis EC1-00500
FDA UDI
Class IIActive
Mis MC1-00470
FDA UDI
Class IIActive
Mis MT-HMR25
FDA UDI
Class IUnknown
Mis MF5-10600
FDA UDI
Class IIActive
Mis MH-N4330
FDA UDI
Class IIActive
Mis CS-AT002
FDA UDI
Class IIActive
Mis CK-SLC3
FDA UDI
Class IIActive
Mis MA-WO303
FDA UDI
Class IIActive
Mis MF5-13420
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