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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 37 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CK-WLC3
FDA UDI
Class IIActive
Mis M5C-11375
FDA UDI
Class IIActive
Mis MW-CCI10
FDA UDI
Class IIActive
Mis MT-TDN32
FDA UDI
Class IActive
Mis MD-IT340
FDA UDI
Class IActive
Mis VK-NPK44-USA
FDA UDI
Class IIUnknown
Mis CS-H0839
FDA UDI
Class IIActive
Mis MD-GT190
FDA UDI
Class IUnknown
Mis MT-S5006
FDA UDI
Class IUnknown
Mis MM-G0330
FDA UDI
Class IIActive
MIS Equator CK-NOE2
FDA UDI
Class IIActive
Mis M5C-16420
FDA UDI
Class IIActive
Mis CK-CPK43
FDA UDI
Class IIActive
Mis MK-XD01
FDA UDI
Class IActive
Mis MT-S3208
FDA UDI
Class IActive
Mis MT-HDL30
FDA UDI
Class IActive
Mis MT-LOC10
FDA UDI
Class IActive
Mis MN-CPK62
FDA UDI
Class IIUnknown
Mis CS-HS475
FDA UDI
Class IIActive
Mis CN-GPC10
FDA UDI
Class IIActive
MIS Multi Unit MA-N3480
FDA UDI
Class IIActive
Mis MM-PBU10
FDA UDI
Class IIActive
Mis EH-W5630
FDA UDI
Class IIActive
Mis MT-BTT50
FDA UDI
Class IActive
Mis LNXC-08500
FDA UDI
Class IIActive
Mis MT-S2410
FDA UDI
Class IActive
Mis MF7-D10500
FDA UDI
Class IIActive
Mis VN-RSM10
FDA UDI
Class IActive
Mis CK-SPZ4
FDA UDI
Class IIUnknown
Mis ED-P0030
FDA UDI
Class IIUnknown
Mis MA-NC448
FDA UDI
Class IIActive
Mis C1-D13420
FDA UDI
Class IIActive
Mis CG-D1139
FDA UDI
Class IActive
Mis MG-NS040
FDA UDI
Class IActive
Mis MM-CP045
FDA UDI
Class IIUnknown
Mis C1-D08375
FDA UDI
Class IIActive
Mis MD-CP013
FDA UDI
Class IIActive
Mis MK-WPK42
FDA UDI
Class IIActive
Mis MT-BTT28
FDA UDI
Class IActive
Mis MT-00600
FDA UDI
Class IActive
Mis MD-TPH50
FDA UDI
Class IIActive
Mis MT-IE172
FDA UDI
Class IUnknown
Mis CT-SSI10
FDA UDI
Class IActive
Mis MT-MUL02
FDA UDI
Class IActive
Mis CK-CPK84-USA
FDA UDI
Class IIActive
Mis ED-CPK61
FDA UDI
Class IIUnknown
Mis C1 C1-11420
FDA UDI
Class IIActive
Mis MD-S0222
FDA UDI
Class IIActive
Mis VS-P8255
FDA UDI
Class IIActive
Mis C1-D16500
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