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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
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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 21 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis M5C-10500
FDA UDI
Class IIActive
Mis VN-AT202
FDA UDI
Class IIActive
Mis MD-GPH13
FDA UDI
Class IIUnknown
Mis MT-S4013
FDA UDI
Class IUnknown
Mis MN-LOC03
FDA UDI
Class IIActive
Mis MG-D0650
FDA UDI
Class IActive
Mis MK-NLC2
FDA UDI
Class IIActive
Mis CN-HS440
FDA UDI
Class IIActive
Mis MT-S4513
FDA UDI
Class IActive
Mis M7C-16500
FDA UDI
Class IIActive
Mis MK-SLC1
FDA UDI
Class IIActive
Mis MD-CPK81
FDA UDI
Class IIActive
Mis EK-CPK63
FDA UDI
Class IIActive
Mis CS-H0639
FDA UDI
Class IIActive
Mis CN-CIZ60
FDA UDI
Class IIActive
Mis MT-SM005
FDA UDI
Class IActive
Mis M4 MF4-16330
FDA UDI
Class IIActive
Mis MT-HK100
FDA UDI
Class IActive
Mis CG-GMN10
FDA UDI
Class IActive
Mis VK-NPK64
FDA UDI
Class IIActive
Mis MW-CP060
FDA UDI
Class IIActive
Mis MD-AT253
FDA UDI
Class IIActive
Mis CW-HS655
FDA UDI
Class IIActive
Mis C1-D13500
FDA UDI
Class IIActive
Mis MU-CC481
FDA UDI
Class IIActive
Mis EW-CPK64
FDA UDI
Class IIActive
Mis CT-WLI10
FDA UDI
Class IActive
Mis CW-C4040
FDA UDI
Class IIActive
Mis MD-P2530
FDA UDI
Class IIActive
Mis MT-HW001
FDA UDI
Class IUnknown
Mis CN-IN060
FDA UDI
Class IIActive
Mis MG-D1033
FDA UDI
Class IActive
Mis MN-I0330
FDA UDI
Class IActive
Mis CG-NTAS0
FDA UDI
Class IActive
Mis CT-SLM30
FDA UDI
Class IActive
Mis MW-TC023
FDA UDI
Class IIActive
Mis MK-SLC5
FDA UDI
Class IIActive
Mis MT-CS500
FDA UDI
Class IActive
Mis M7C-06500
FDA UDI
Class IIActive
Mis VN-SP102
FDA UDI
Class IActive
Mis V3-16390
FDA UDI
Class IIActive
Mis CS-C2040
FDA UDI
Class IIActive
Mis CN-TB015
FDA UDI
Class IIActive
Mis MT-HLI20
FDA UDI
Class IActive
Mis C1 C1-10375
FDA UDI
Class IIActive
Mis V3-16500
FDA UDI
Class IIActive
Mis VN-IC401
FDA UDI
Class IActive
Mis MD-S0200
FDA UDI
Class IIActive
Mis MD-AN151
FDA UDI
Class IIActive
Mis CT-SADL1
FDA UDI
Class IUnknown

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