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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 36 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MW-IO551
FDA UDI
Class IActive
Mis MG-NRS10
FDA UDI
Class IActive
Mis CT-NLR10
FDA UDI
Class IActive
Mis CW-AT153
FDA UDI
Class IIActive
Mis CF5-11330
FDA UDI
Class IIActive
Mis MG-SD01
FDA UDI
Class IActive
Mis CD-G0200
FDA UDI
Class IUnknown
Mis MN-CC010
FDA UDI
Class IIActive
Mis MG-K004
FDA UDI
Class IActive
Mis VN-P6140
FDA UDI
Class IIActive
Mis V3-10390
FDA UDI
Class IIActive
Mis CB-00225
FDA UDI
Class IIActive
Mis MM-H1557
FDA UDI
Class IIActive
MIS Equator ED-OE541
FDA UDI
Class IIUnknown
MIS Multi Unit MA-S4480
FDA UDI
Class IIActive
Mis ED-TPH50
FDA UDI
Class IIUnknown
MIS Multi Unit MA-N2480
FDA UDI
Class IIActive
Mis Seven MF7-10600
FDA UDI
Class IIActive
Mis EW-CPH13
FDA UDI
Class IIActive
Mis MF5-11500
FDA UDI
Class IIActive
Mis CW-C1540
FDA UDI
Class IIActive
Mis MN-ITC30
FDA UDI
Class IActive
Mis CK-SPC4
FDA UDI
Class IIActive
Mis MT-BT050
FDA UDI
Class IActive
Mis VN-PF340
FDA UDI
Class IActive
Mis Mistral MF9-16410
FDA UDI
Class IIActive
Mis MG-DFP20
FDA UDI
Class IActive
Mis MM-H0540
FDA UDI
Class IIActive
Mis MG-GRI01
FDA UDI
Class IActive
Mis MB-NR005
FDA UDI
Class IIUnknown
Mis Lance EF5-10420
FDA UDI
Class IIActive
Mis MG-N0833
FDA UDI
Class IActive
Mis CG-NMS10
FDA UDI
Class IActive
Mis LT-WLR10
FDA UDI
Class IActive
Mis V3C-16390
FDA UDI
Class IIActive
Mis MD-TC013
FDA UDI
Class IIActive
Mis M5C-08600
FDA UDI
Class IIActive
Mis MT-P2408
FDA UDI
Class IUnknown
Mis MG-K005
FDA UDI
Class IActive
Mis CN-H0333
FDA UDI
Class IIActive
Mis MD-TPA10
FDA UDI
Class IIActive
Mis M4 MF4-08420
FDA UDI
Class IIActive
Mis MD-IO481
FDA UDI
Class IActive
Mis MK-NPK62
FDA UDI
Class IIActive
Mis MG-SI455
FDA UDI
Class IActive
Mis MG-D1133
FDA UDI
Class IActive
Mis VK-NPK62-USA
FDA UDI
Class IIUnknown
Mis ED-CPK41
FDA UDI
Class IIUnknown
Mis MM-LLR10
FDA UDI
Class IIUnknown
Mis M5C-11420
FDA UDI
Class IIActive

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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