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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
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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 22 of 42
DeviceModel / ReferenceRegistriesClassStatus
MIS Locator MB-NZL04
FDA UDI
Class IIUnknown
MIS Locator MB-WZL05
FDA UDI
Class IIUnknown
Mis VK-NPK61-USA
FDA UDI
Class IIActive
Mis M7C-10330
FDA UDI
Class IIActive
Mis 4bone 4B-C2030
FDA UDI
Class IIActive
MIS Equator MK-NOE1
FDA UDI
Class IIActive
Mis CW-HS450
FDA UDI
Class IIActive
Mis VS-AT003
FDA UDI
Class IIActive
Mis MM-TRU10
FDA UDI
Class IIActive
Mis EH-04410
FDA UDI
Class IIActive
Mis EK-WPK42
FDA UDI
Class IIUnknown
Mis MB-TTP10
FDA UDI
Class IIActive
Mis LNXC-10375
FDA UDI
Class IIActive
Mis MG-K002
FDA UDI
Class IActive
Mis MW-TCH33
FDA UDI
Class IIActive
Mis EK-WPK44
FDA UDI
Class IIUnknown
MIS Multi Unit MA-W4500
FDA UDI
Class IIUnknown
Mis CW-HA263
FDA UDI
Class IIActive
Mis ED-S0222
FDA UDI
Class IIActive
Mis CK-NLC2
FDA UDI
Class IIActive
Mis MC3-00470
FDA UDI
Class IIActive
Mis VN-IO335
FDA UDI
Class IActive
Mis MW-IB951
FDA UDI
Class IIUnknown
Mis Uno MO1-11300
FDA UDI
Class IIActive
Mis MT-SRH21
FDA UDI
Class IActive
Mis MN-TPA10
FDA UDI
Class IIActive
Mis CK-SLC2
FDA UDI
Class IIActive
Mis CS-TC033
FDA UDI
Class IIActive
Mis EW-CPK83
FDA UDI
Class IIUnknown
Mis ED-P2530
FDA UDI
Class IIUnknown
Mis MM-LELE1
FDA UDI
Class IIUnknown
Mis MM-IO057
FDA UDI
Class IActive
Mis ED-TC013
FDA UDI
Class IIUnknown
Mis CN-C3040
FDA UDI
Class IIActive
Mis MB-TBS20
FDA UDI
Class IUnknown
Mis MK-NLC3
FDA UDI
Class IIActive
MIS Ball Attachment MB-N2330
FDA UDI
Class IIActive
Mis CN-AN010
FDA UDI
Class IIActive
Mis EM-SA001
FDA UDI
Class IIUnknown
Mis LT-SSR10
FDA UDI
Class IActive
Mis Uno MO1-10300
FDA UDI
Class IIActive
Mis CN-TPA10
FDA UDI
Class IIActive
Mis MG-D1324
FDA UDI
Class IActive
Mis CG-D0850
FDA UDI
Class IActive
Mis MW-IC800
FDA UDI
Class IActive
Mis Uno MO1-16300
FDA UDI
Class IIActive
Mis MH-W0455
FDA UDI
Class IIActive
Mis MT-TDN28
FDA UDI
Class IActive
Mis CS-C1540
FDA UDI
Class IIActive
Mis ED-CPK83
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