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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 41 of 42
DeviceModel / ReferenceRegistriesClassStatus
MIS Locator MB-SZL01
FDA UDI
Class IIUnknown
Mis MH-56375
FDA UDI
Class IIActive
Mis VS-TCI23
FDA UDI
Class IIActive
Mis MK-NLC4
FDA UDI
Class IIActive
Mis CN-LOC01
FDA UDI
Class IIActive
MIS Locator MB-NZL06
FDA UDI
Class IIActive
Mis CK-NPK44
FDA UDI
Class IIActive
Mis MA-SO302
FDA UDI
Class IIActive
Mis MW-TPA10
FDA UDI
Class IIActive
Mis CN-CPK43
FDA UDI
Class IIActive
Mis MT-HKO21
FDA UDI
Class IUnknown
Mis CN-H0533
FDA UDI
Class IIActive
Mis MA-NO302
FDA UDI
Class IIActive
Mis MT-MFXSS
FDA UDI
Class IActive
Mis MG-KT04
FDA UDI
Class IActive
Mis VK-NPK44
FDA UDI
Class IIActive
Mis MN-G0160
FDA UDI
Class IUnknown
Mis MN-ICH40
FDA UDI
Class IActive
MIS Equator MK-SOE2
FDA UDI
Class IIActive
Mis V3C-08500
FDA UDI
Class IIActive
Mis MW-TCH23
FDA UDI
Class IIActive
MIS Locator MB-NZL05
FDA UDI
Class IIActive
Mis M7C-16420
FDA UDI
Class IIActive
Mis MG-N1133
FDA UDI
Class IActive
Mis MH-03375
FDA UDI
Class IIActive
Mis MG-NMS10
FDA UDI
Class IActive
MIS Ti Base MD-TB001
FDA UDI
Class IIActive
MIS Multi Unit CM-N5480
FDA UDI
Class IIActive
Mis MF4-18420
FDA UDI
Class IIUnknown
Mis MT-CS330
FDA UDI
Class IActive
Mis MG-D1650
FDA UDI
Class IActive
Mis EW-CPK44
FDA UDI
Class IIUnknown
Mis MT-LBT28
FDA UDI
Class IActive
MIS Equator CS-OE137
FDA UDI
Class IIActive
Mis C1C-08500
FDA UDI
Class IIActive
Mis MC3-00330
FDA UDI
Class IIActive
Mis MT-S3013
FDA UDI
Class IUnknown
Mis CK-CPK83-USA
FDA UDI
Class IIUnknown
Mis CT-NLM30
FDA UDI
Class IActive
Mis CN-IN160
FDA UDI
Class IIActive
Mis MM-LMP02
FDA UDI
Class IIActive
Mis MH-A3375
FDA UDI
Class IIActive
Mis MH-54330
FDA UDI
Class IIActive
Mis CW-TPA10
FDA UDI
Class IIActive
MIS Ball Attachment CN-B4330
FDA UDI
Class IIActive
Mis MG-D1042
FDA UDI
Class IActive
Mis MT-ELM10
FDA UDI
Class IActive
MIS Locator MB-NZL03
FDA UDI
Class IIUnknown
Mis MK-0058
FDA UDI
Class IActive
Mis EK-CPK84
FDA UDI
Class IIUnknown

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