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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 27 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MT-BTL31
FDA UDI
Class IActive
Mis MT-SMD10
FDA UDI
Class IActive
Mis M4 MF4-16420
FDA UDI
Class IIActive
Mis MM-LBP10
FDA UDI
Class IIUnknown
Mis Seven MG7-10330
FDA UDI
Class IIActive
Mis CS-TB030
FDA UDI
Class IIActive
Mis MG-D0837
FDA UDI
Class IActive
Mis VG-NRN01
FDA UDI
Class IActive
Mis CW-HA363
FDA UDI
Class IIActive
Mis CF5-11375
FDA UDI
Class IIActive
Mis MW-CC010
FDA UDI
Class IIActive
Mis CW-IO555
FDA UDI
Class IActive
Mis C1-D16330
FDA UDI
Class IIActive
MIS Equator EW-OE350
FDA UDI
Class IIUnknown
Mis ED-P1530
FDA UDI
Class IIUnknown
Mis MH-S0548
FDA UDI
Class IIActive
Mis VK-CPK81
FDA UDI
Class IIActive
Mis MT-PDM24
FDA UDI
Class IActive
Mis MU-S0220
FDA UDI
Class IIActive
Mis VN-AT102
FDA UDI
Class IIActive
Mis MG-N1033
FDA UDI
Class IActive
Mis VG-GRN10
FDA UDI
Class IActive
Mis CG-N1139
FDA UDI
Class IActive
Mis CF5-13420
FDA UDI
Class IIActive
Mis C1 C1-08375
FDA UDI
Class IIActive
Mis MG-N1624
FDA UDI
Class IActive
Mis GI-WCH11
FDA UDI
Class IActive
Mis MT-S3510
FDA UDI
Class IActive
Mis CS-CPK81
FDA UDI
Class IIActive
Mis M7C-16330
FDA UDI
Class IIActive
Mis MT-TDI55
FDA UDI
Class IActive
Mis Uno MO1-11350
FDA UDI
Class IIActive
MIS Ti Base MK-TBW4
FDA UDI
Class IIUnknown
Mis MT-CDS20
FDA UDI
Class IUnknown
Mis MG-D0824
FDA UDI
Class IActive
Mis ED-MAC10
FDA UDI
Class IIUnknown
Mis CM-NO171
FDA UDI
Class IIActive
MIS Multi Unit MA-S1480
FDA UDI
Class IIActive
Mis MK-CPK43
FDA UDI
Class IIActive
Mis MT-TDN45
FDA UDI
Class IActive
Mis MW-RSM60
FDA UDI
Class IActive
Mis Seven MF7-13500
FDA UDI
Class IIActive
Mis CS-CPK64
FDA UDI
Class IIActive
Mis MD-P0030
FDA UDI
Class IIActive
Mis M4 MF4-13500
FDA UDI
Class IIActive
Mis MF5-10420
FDA UDI
Class IIActive
Mis C1C-13330
FDA UDI
Class IIActive
Mis MM-TC100
FDA UDI
Class IIUnknown
MIS Equator MK-NOE4
FDA UDI
Class IIActive
Mis MK-WPC63
FDA UDI
Class IIActive

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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