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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
—
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 24 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CN-HA448
FDA UDI
Class IIActive
Mis CS-IN160
FDA UDI
Class IIActive
Mis MT-HSI10
FDA UDI
Class IActive
Mis MD-ITC30
FDA UDI
Class IActive
Mis Lance EF5-16500
FDA UDI
Class IIActive
Mis CK-WPK84
FDA UDI
Class IIUnknown
Mis MT-C2416
FDA UDI
Class IActive
Mis M4 MF4-11420
FDA UDI
Class IIActive
Mis CF5-11500
FDA UDI
Class IIActive
Mis MF5-08420
FDA UDI
Class IIActive
Mis Seven MF7-08375
FDA UDI
Class IIActive
Mis M7C-11375
FDA UDI
Class IIActive
Mis MG-TP055
FDA UDI
Class IActive
MIS Equator EK-WOE3
FDA UDI
Class IIUnknown
Mis MG-P1124
FDA UDI
Class IActive
Mis MG-N1333
FDA UDI
Class IActive
Mis MW-CPC64
FDA UDI
Class IIActive
MIS Ball Attachment MB-N3330
FDA UDI
Class IIActive
MIS Equator EK-SOE4
FDA UDI
Class IIUnknown
Mis TD-RS240
FDA UDI
Class IUnknown
Mis MT-TDN35
FDA UDI
Class IActive
Mis CF5-08500
FDA UDI
Class IIActive
Mis CS-LOC04
FDA UDI
Class IIActive
Mis MD-GP100
FDA UDI
Class IUnknown
Mis MK-WPK84
FDA UDI
Class IIActive
Mis MT-S5008
FDA UDI
Class IUnknown
Mis CS-IO391
FDA UDI
Class IActive
Mis MU-MAN10
FDA UDI
Class IActive
Mis MK-WPC4
FDA UDI
Class IIActive
Mis CS-CPK41
FDA UDI
Class IIActive
Mis MT-S3813
FDA UDI
Class IActive
Mis MT-MUK02
FDA UDI
Class IUnknown
Mis MT-RDL30
FDA UDI
Class IActive
MIS Ball Attachment EB-N2410
FDA UDI
Class IIUnknown
Mis CK-CPK81-USA
FDA UDI
Class IIActive
Mis MG-NMN10
FDA UDI
Class IActive
Mis Mistral MF9-08410
FDA UDI
Class IIActive
Mis MT-MSM30
FDA UDI
Class IActive
Mis MK-CD01
FDA UDI
Class IActive
Mis CN-TCI33
FDA UDI
Class IIActive
Mis MM-H0557
FDA UDI
Class IIActive
Mis Seven MF7-16500
FDA UDI
Class IIActive
Mis M5C-16375
FDA UDI
Class IIActive
Mis CG-GMS10
FDA UDI
Class IActive
Mis MT-MURS2
FDA UDI
Class IActive
Mis C1C-11420
FDA UDI
Class IIActive
MIS Ti Base MW-TB002
FDA UDI
Class IIActive
Mis MW-CPK84
FDA UDI
Class IIActive
Mis MA-SO173
FDA UDI
Class IIActive
Mis MT-TDI38
FDA UDI
Class IActive

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