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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 32 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CG-NRN01
FDA UDI
Class IActive
Mis MT-HSI20
FDA UDI
Class IUnknown
Mis CW-LOC03
FDA UDI
Class IIActive
Mis CW-MAB10
FDA UDI
Class IActive
Mis CF5C-13330
FDA UDI
Class IIActive
Mis M5C-11600
FDA UDI
Class IIActive
Mis MT-HSI21
FDA UDI
Class IActive
Mis MD-IB121
FDA UDI
Class IIUnknown
MIS Multi Unit CM-W5480
FDA UDI
Class IIActive
Mis CS-CPK63
FDA UDI
Class IIActive
Mis Seven MF7-16330
FDA UDI
Class IIActive
Mis MG-N0633
FDA UDI
Class IActive
MIS Locator MB-SZL00
FDA UDI
Class IIUnknown
Mis EK-CPK62
FDA UDI
Class IIUnknown
Mis Lance EF5-11420
FDA UDI
Class IIActive
Mis CW-AT253
FDA UDI
Class IIActive
Mis CW-IO505
FDA UDI
Class IActive
Mis MT-RDS30
FDA UDI
Class IActive
MIS Equator MK-WOE5
FDA UDI
Class IIActive
Mis MF7-D13500
FDA UDI
Class IIActive
Mis MK-0011
FDA UDI
Class IUnknown
Mis MU-CP048
FDA UDI
Class IIActive
Mis CS-C1557
FDA UDI
Class IIActive
Mis M7C-11330
FDA UDI
Class IIActive
Mis CN-GP010
FDA UDI
Class IIActive
Mis MK-SIC6
FDA UDI
Class IIUnknown
Mis MT-BTL49
FDA UDI
Class IActive
Mis CC1-00375
FDA UDI
Class IIActive
Mis MF7-D10330
FDA UDI
Class IIActive
Mis V3-13430
FDA UDI
Class IIActive
Mis MD-CPK63
FDA UDI
Class IIUnknown
Mis MG-TAS55
FDA UDI
Class IActive
Mis CT-WSR10
FDA UDI
Class IActive
Mis VK-NPK61
FDA UDI
Class IIActive
Mis MU-T0480
FDA UDI
Class IIUnknown
Mis MF7-D16500
FDA UDI
Class IIActive
MIS Ball Attachment CW-B5500
FDA UDI
Class IIActive
MIS Ball Attachment MB-AN152
FDA UDI
Class IIActive
Mis MM-LER10
FDA UDI
Class IIActive
Mis Seven MF7-08500
FDA UDI
Class IIActive
Mis CS-MC103
FDA UDI
Class IIActive
Mis MN-IO401
FDA UDI
Class IActive
Mis LT-WLM10
FDA UDI
Class IActive
Mis Seven MF7-08600
FDA UDI
Class IIActive
Mis CN-AN001
FDA UDI
Class IIActive
Mis CA-S0002
FDA UDI
Class IIUnknown
Mis CW-TC033
FDA UDI
Class IIActive
Mis MF7-D10420
FDA UDI
Class IIActive
Mis EK-WPK43
FDA UDI
Class IIUnknown
Mis CK-WPK82
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