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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
—
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 11 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MG-D1024
FDA UDI
Class IActive
Mis MT-SPP24
FDA UDI
Class IActive
Mis CW-TB002
FDA UDI
Class IIActive
Mis MT-TDI30
FDA UDI
Class IActive
MIS Multi Unit CM-S3480
FDA UDI
Class IIActive
Mis C1 C1-10500
FDA UDI
Class IIActive
Mis MM-TCI40
FDA UDI
Class IIUnknown
Mis MW-CPK43
FDA UDI
Class IIUnknown
Mis MT-ETD38
FDA UDI
Class IActive
Mis MG-D1633
FDA UDI
Class IActive
Mis ED-CPK82
FDA UDI
Class IIUnknown
Mis C1 C1-11500
FDA UDI
Class IIActive
Mis 4bone 4B-X1010
FDA UDI
Class IIActive
Mis C1 C1C-08375
FDA UDI
Class IIActive
Mis M7C-08600
FDA UDI
Class IIActive
Mis MK-SPC4
FDA UDI
Class IIUnknown
Mis MG-N0624
FDA UDI
Class IActive
Mis CG-D1143
FDA UDI
Class IActive
Mis CN-IC405
FDA UDI
Class IActive
Mis CN-IN260
FDA UDI
Class IIUnknown
Mis MM-CFI54
FDA UDI
Class IIActive
Mis VG-NRS10
FDA UDI
Class IActive
Mis ED-RSM10
FDA UDI
Class IUnknown
Mis CG-GRW10
FDA UDI
Class IActive
Mis MW-I0470
FDA UDI
Class IActive
MIS Multi Unit CM-N3480
FDA UDI
Class IIActive
Mis MF5-11420
FDA UDI
Class IIActive
Mis MG-P0624
FDA UDI
Class IActive
Mis MF5-11375
FDA UDI
Class IIActive
Mis MG-D1137
FDA UDI
Class IActive
Mis VN-IO331
FDA UDI
Class IActive
Mis MW-IB121
FDA UDI
Class IIUnknown
Mis MK-MCPS1
FDA UDI
Class IIUnknown
Mis CN-LOC02
FDA UDI
Class IIActive
Mis VN-MC103
FDA UDI
Class IIActive
Mis MH-W3500
FDA UDI
Class IIActive
Mis MF7-D08375
FDA UDI
Class IIActive
Mis M4 MF4-11375
FDA UDI
Class IIActive
Mis CK-CPK83
FDA UDI
Class IIActive
Mis CK-CPK82
FDA UDI
Class IIActive
Mis MM-H1540
FDA UDI
Class IIActive
Mis EH-55410
FDA UDI
Class IIActive
Mis CK-CPK44-USA
FDA UDI
Class IIUnknown
Mis ED-CPK43
FDA UDI
Class IIActive
Mis MA-WO302
FDA UDI
Class IIActive
Mis MK-SLC3
FDA UDI
Class IIActive
Mis MH-N6330
FDA UDI
Class IIActive
Mis CF5-10375
FDA UDI
Class IIActive
Mis MT-RI040
FDA UDI
Class IActive
Mis MT-TDN40
FDA UDI
Class IActive

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