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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
—
LinkedIn
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Facebook
—
Email
—
Phone
—
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 5 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MF5-08600
FDA UDI
Class IIActive
Mis MW-AN151
FDA UDI
Class IIActive
Mis CD-CA420
FDA UDI
Class IIUnknown
Mis MN-IN060
FDA UDI
Class IIActive
Mis MD-TBC30
FDA UDI
Class IIActive
Mis MK-0041
FDA UDI
Class IActive
Mis MU-MG480
FDA UDI
Class IIActive
Mis Lance EF5-16420
FDA UDI
Class IIActive
MIS Multi Unit CM-SA301
FDA UDI
Class IIActive
Mis MT-RT002
FDA UDI
Class IActive
Mis MN-PF330
FDA UDI
Class IActive
Mis CK-CPK42-USA
FDA UDI
Class IIUnknown
Mis VK-NPK43
FDA UDI
Class IIActive
Mis C1 C1-13420
FDA UDI
Class IIActive
Mis MW-CPK44
FDA UDI
Class IIActive
Mis MU-G0220
FDA UDI
Class IIActive
MIS Ball Attachment EB-N3410
FDA UDI
Class IIUnknown
Mis MD-LOC02
FDA UDI
Class IIActive
Mis CN-AN310
FDA UDI
Class IIActive
Mis MH-W5630
FDA UDI
Class IIActive
Mis MG-NRN10
FDA UDI
Class IActive
Mis CK-WPZ4
FDA UDI
Class IIUnknown
Mis MA-SC348
FDA UDI
Class IIActive
Mis M5C-08375
FDA UDI
Class IIActive
Mis CN-CPK64
FDA UDI
Class IIActive
Mis CM-WO301
FDA UDI
Class IIActive
MIS Equator CS-OE437
FDA UDI
Class IIUnknown
Mis CM-SO172
FDA UDI
Class IIActive
Mis V3C-08430
FDA UDI
Class IIActive
Mis CW-GP010
FDA UDI
Class IIActive
Mis MN-CPC62
FDA UDI
Class IIActive
Mis CF5-13375
FDA UDI
Class IIActive
Mis MK-NPK61
FDA UDI
Class IIActive
Mis CS-IN360
FDA UDI
Class IIActive
Mis MG-NTP40
FDA UDI
Class IActive
Mis CW-C4057
FDA UDI
Class IIActive
Mis CN-RSM10
FDA UDI
Class IActive
Mis VS-HS558
FDA UDI
Class IIActive
Mis VN-P6240
FDA UDI
Class IIActive
Mis C1-D10500
FDA UDI
Class IIActive
Mis M5C-08500
FDA UDI
Class IIActive
Mis C1-D10420
FDA UDI
Class IIActive
Mis CS-H0339
FDA UDI
Class IIActive
MIS Ball Attachment EB-N4410
FDA UDI
Class IIUnknown
Mis CT-SSR10
FDA UDI
Class IActive
Mis MD-TCH33
FDA UDI
Class IIActive
Mis CG-GRN01
FDA UDI
Class IActive
Mis MT-LMK09
FDA UDI
Class IActive
MIS Multi Unit MA-W3480
FDA UDI
Class IIActive
Mis CA-GTC10
FDA UDI
Class IIUnknown

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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