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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 16 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CN-LOC04
FDA UDI
Class IIActive
Mis MF5-10500
FDA UDI
Class IIActive
Mis CN-HS633
FDA UDI
Class IIActive
Mis CW-HA350
FDA UDI
Class IIActive
Mis CK-CPK84
FDA UDI
Class IIActive
Mis CM-WO302
FDA UDI
Class IIActive
Mis MT-S4510
FDA UDI
Class IUnknown
Mis CN-AN020
FDA UDI
Class IIActive
Mis Seven MF7-11500
FDA UDI
Class IIActive
Mis MT-MRH20
FDA UDI
Class IUnknown
Mis MW-AT152
FDA UDI
Class IIActive
Mis CW-SP102
FDA UDI
Class IActive
Mis MW-CPK83
FDA UDI
Class IIUnknown
Mis MF7-20420
FDA UDI
Class IIActive
Mis MM-MAN40
FDA UDI
Class IActive
Mis CK-NPK64
FDA UDI
Class IIActive
Mis CN-HS433
FDA UDI
Class IIActive
Mis MK-0026
FDA UDI
Class IUnknown
Mis CG-D1639
FDA UDI
Class IActive
Mis EH-W3500
FDA UDI
Class IIActive
Mis M4 MF4-11500
FDA UDI
Class IIActive
Mis VN-AT003
FDA UDI
Class IIActive
MIS Multi Unit MA-N5480
FDA UDI
Class IIActive
Mis EH-03410
FDA UDI
Class IIActive
Mis MW-CPK81
FDA UDI
Class IIUnknown
MIS Locator MB-SZL06
FDA UDI
Class IIUnknown
Mis MH-00450
FDA UDI
Class IIUnknown
Mis EW-GP010
FDA UDI
Class IIUnknown
MIS Equator MK-SOE1
FDA UDI
Class IIActive
Mis V3-08430
FDA UDI
Class IIActive
Mis MW-LOC05
FDA UDI
Class IIActive
Mis CM-SO301
FDA UDI
Class IIActive
Mis MD-P1530
FDA UDI
Class IIActive
Mis LNXC-16420
FDA UDI
Class IIActive
Mis M5C-10330
FDA UDI
Class IIActive
Mis CN-I0330
FDA UDI
Class IActive
MIS Locator MB-SZL05
FDA UDI
Class IIUnknown
Mis MN-IB951
FDA UDI
Class IIUnknown
Mis MK-CPK63
FDA UDI
Class IIActive
Mis MD-CPH13
FDA UDI
Class IIActive
Mis CS-C4057
FDA UDI
Class IIActive
MIS Multi Unit MA-WA301
FDA UDI
Class IIActive
Mis MT-BTT45
FDA UDI
Class IActive
Mis VN-P4340
FDA UDI
Class IIActive
Mis M5C-11500
FDA UDI
Class IIActive
Mis VK-NPK62
FDA UDI
Class IIActive
Mis CF5C-10375
FDA UDI
Class IIActive
MIS Equator CW-OE150
FDA UDI
Class IIActive
Mis CA-GS001
FDA UDI
Class IIActive
MIS Multi Unit CM-S4480
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