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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 38 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CS-GPC10
FDA UDI
Class IIActive
Mis CT-BP460
FDA UDI
Class IUnknown
Mis CW-TBF15
FDA UDI
Class IIActive
Mis CS-H0539
FDA UDI
Class IIActive
Mis EK-WPK61
FDA UDI
Class IIActive
Mis MT-BTL41
FDA UDI
Class IActive
Mis MG-BM055
FDA UDI
Class IActive
Mis EB-RS410
FDA UDI
Class IUnknown
Mis CG-D1150
FDA UDI
Class IActive
Mis Seven MF7-10420
FDA UDI
Class IIActive
Mis CW-CPK63
FDA UDI
Class IIActive
Mis MM-CLE10
FDA UDI
Class IActive
MIS Multi Unit MA-S2375
FDA UDI
Class IIActive
Mis VS-TC013
FDA UDI
Class IIActive
Mis MN-TC023
FDA UDI
Class IIActive
Mis M4 MF4-10420
FDA UDI
Class IIActive
Mis MD-MC102
FDA UDI
Class IIActive
Mis MK-EI48
FDA UDI
Class IUnknown
Mis MG-D0624
FDA UDI
Class IActive
Mis VK-CPK62-USA
FDA UDI
Class IIActive
Mis CK-CPK43-USA
FDA UDI
Class IIUnknown
Mis MB-PPC10
FDA UDI
Class IActive
Mis MM-SP105
FDA UDI
Class IActive
Mis MT-S3806
FDA UDI
Class IActive
Mis ED-CPK42
FDA UDI
Class IIUnknown
Mis MT-TDI40
FDA UDI
Class IActive
Mis MG-FP020
FDA UDI
Class IActive
Mis MK-NPK64
FDA UDI
Class IIActive
Mis CF5C-16375
FDA UDI
Class IIActive
Mis Mistral MF9-11410
FDA UDI
Class IIActive
Mis CS-A2530
FDA UDI
Class IIActive
Mis MN-RSM60
FDA UDI
Class IActive
Mis CS-IN060
FDA UDI
Class IIActive
Mis MT-S3213
FDA UDI
Class IActive
Mis MT-NB225
FDA UDI
Class IActive
Mis Uno MO1-13350
FDA UDI
Class IIActive
Mis MK-0056
FDA UDI
Class IActive
Mis 4matrix BS-4MX10
FDA UDI
Class IIActive
MIS Multi Unit MA-ANH30
FDA UDI
Class IIActive
Mis MK-WPK62
FDA UDI
Class IIActive
Mis CD-SA550
FDA UDI
Class IIUnknown
Mis CF5C-08375
FDA UDI
Class IIActive
Mis CN-HS333
FDA UDI
Class IIActive
Mis MT-S5011
FDA UDI
Class IUnknown
Mis MT-S5013
FDA UDI
Class IUnknown
Mis M7C-10375
FDA UDI
Class IIActive
Mis MK-NPK43
FDA UDI
Class IIActive
Mis MN-LOC04
FDA UDI
Class IIActive
Mis MT-S3810
FDA UDI
Class IActive
Mis VM-NO171
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