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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
—
LinkedIn
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Facebook
—
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 10 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MF7-D10375
FDA UDI
Class IIActive
Mis C1 C1-11330
FDA UDI
Class IIActive
Mis MD-IT100
FDA UDI
Class IActive
Mis MM-TC041
FDA UDI
Class IIActive
Mis V3C-11500
FDA UDI
Class IIActive
Mis CW-AT251
FDA UDI
Class IIActive
Mis CW-TPH50
FDA UDI
Class IIUnknown
Mis MW-CPK82
FDA UDI
Class IIActive
Mis MK-CDS11
FDA UDI
Class IActive
Mis MD-RSM10
FDA UDI
Class IActive
Mis MG-N0637
FDA UDI
Class IActive
Mis MT-AL002
FDA UDI
Class IUnknown
Mis V3-11390
FDA UDI
Class IIActive
Mis M7C-10500
FDA UDI
Class IIActive
Mis CS-HA675
FDA UDI
Class IIActive
Mis MM-TCI41
FDA UDI
Class IIActive
Mis Seven MF7-06420
FDA UDI
Class IIActive
Mis CS-B4375
FDA UDI
Class IIActive
Mis V3C-10330
FDA UDI
Class IIActive
Mis MT-HMR10
FDA UDI
Class IUnknown
Mis CK-SLC5
FDA UDI
Class IIActive
Mis MM-TC057
FDA UDI
Class IIActive
Mis MD-CPK42
FDA UDI
Class IIUnknown
Mis MG-D1150
FDA UDI
Class IActive
Mis ED-CPK44
FDA UDI
Class IIUnknown
Mis ET-IT002
FDA UDI
Class IActive
Mis CN-IO331
FDA UDI
Class IActive
Mis MT-S3206
FDA UDI
Class IUnknown
Mis MF4-18375
FDA UDI
Class IIActive
Mis VN-AT201
FDA UDI
Class IIActive
Mis VG-GRS10
FDA UDI
Class IActive
Mis MT-TDN50
FDA UDI
Class IActive
Mis MM-CHC60
FDA UDI
Class IIUnknown
Mis MF5-08375
FDA UDI
Class IIActive
Mis MM-ICI40
FDA UDI
Class IActive
Mis MK-NLC1
FDA UDI
Class IIActive
Mis MH-A4375
FDA UDI
Class IIActive
Mis CW-IC555
FDA UDI
Class IActive
Mis MT-BGP32
FDA UDI
Class IUnknown
Mis MM-CF054
FDA UDI
Class IIActive
Mis MT-S3808
FDA UDI
Class IActive
Mis CT-SLI10
FDA UDI
Class IActive
Mis Lance EF5-16375
FDA UDI
Class IIActive
Mis CK-SPS40
FDA UDI
Class IIUnknown
Mis OE-MH001
FDA UDI
Class IActive
Mis MK-BH26
FDA UDI
Class IUnknown
Mis VK-NPK43-USA
FDA UDI
Class IIActive
Mis VN-IN360
FDA UDI
Class IIActive
Mis MW-IT300
FDA UDI
Class IActive
Mis CK-WPK81
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