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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 31 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CS-C4040
FDA UDI
Class IIActive
Mis MW-CTP10
FDA UDI
Class IIActive
Mis MF7-20375
FDA UDI
Class IIUnknown
Mis ED-GP010
FDA UDI
Class IIUnknown
Mis MN-AT102
FDA UDI
Class IIActive
Mis M7C-08375
FDA UDI
Class IIActive
Mis 4bone 4B-X2505
FDA UDI
Class IIActive
Mis MG1-TE480
FDA UDI
Class IActive
Mis M5C-13600
FDA UDI
Class IIActive
Mis CK-NPK42
FDA UDI
Class IIActive
Mis Provisional Implant TF1-B1324
FDA UDI
Class IIActive
Mis CF5C-16500
FDA UDI
Class IIActive
Mis M7C-20420
FDA UDI
Class IIActive
Mis MD-CPC63
FDA UDI
Class IIActive
Mis MT-TDO01
FDA UDI
Class IActive
Mis C1 C1-16330
FDA UDI
Class IIActive
Mis CT-BGP32
FDA UDI
Class IUnknown
Mis CT-SLR30
FDA UDI
Class IActive
Mis MA-SO172
FDA UDI
Class IIActive
Mis MG-US424
FDA UDI
Class IActive
Mis Seven MF7-10375
FDA UDI
Class IIActive
Mis M4 MF4-06600
FDA UDI
Class IIActive
Mis CN-HS840
FDA UDI
Class IIActive
Mis MF5-13500
FDA UDI
Class IIActive
Mis CN-HS233
FDA UDI
Class IIUnknown
Mis M5C-16500
FDA UDI
Class IIActive
Mis MH-55330
FDA UDI
Class IIActive
Mis MD-CPH50
FDA UDI
Class IIActive
Mis EW-CPK61
FDA UDI
Class IIActive
Mis CN-HA648
FDA UDI
Class IIActive
Mis CK-NPK41
FDA UDI
Class IIActive
Mis CK-SLC4
FDA UDI
Class IIActive
Mis VS-MC101
FDA UDI
Class IIActive
Mis EK-WPK82
FDA UDI
Class IIActive
Mis CK-CPK61
FDA UDI
Class IIActive
Mis CS-HS675
FDA UDI
Class IIActive
Mis MD-IC800
FDA UDI
Class IActive
Mis MD-GP0G1
FDA UDI
Class IIUnknown
Mis CN-IO405
FDA UDI
Class IActive
Mis MG-P0824
FDA UDI
Class IActive
Mis MT-LRH20
FDA UDI
Class IActive
Mis EW-CPK41
FDA UDI
Class IIUnknown
Mis MA-NO301
FDA UDI
Class IIActive
Mis MK-T048
FDA UDI
Class IActive
Mis CN-SP102
FDA UDI
Class IActive
Mis Ortho Anchor Screw MG2-10160
FDA UDI
Class IIActive
MIS Equator MK-NOE3
FDA UDI
Class IIActive
Mis MT-ETD24
FDA UDI
Class IActive
Mis MK-WPK44
FDA UDI
Class IIActive
Mis MF5-10375
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