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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
—
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 17 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CM-WO172
FDA UDI
Class IIActive
Mis MT-RT070
FDA UDI
Class IActive
MIS Ball Attachment CN-B3330
FDA UDI
Class IIActive
MIS Equator CK-NOE4
FDA UDI
Class IIActive
Mis V3-10430
FDA UDI
Class IIActive
Mis CN-IO335
FDA UDI
Class IActive
Mis MG-D1050
FDA UDI
Class IActive
Mis MN-SP102
FDA UDI
Class IActive
MIS Equator MK-SOE3
FDA UDI
Class IIActive
Mis MT-LRH21
FDA UDI
Class IActive
Mis ED-S0200
FDA UDI
Class IIActive
Mis MT-CD410
FDA UDI
Class IActive
Mis CG-D1333
FDA UDI
Class IActive
Mis MF7-D06420
FDA UDI
Class IIActive
Mis CS-TPA10
FDA UDI
Class IIActive
Mis MT-00400
FDA UDI
Class IActive
Mis MG-N1637
FDA UDI
Class IActive
Mis MT-S3811
FDA UDI
Class IUnknown
Mis M7C-08420
FDA UDI
Class IIActive
Mis CK-WPK63
FDA UDI
Class IIActive
MIS Locator MB-SZL02
FDA UDI
Class IIActive
Mis MT-RMR10
FDA UDI
Class IActive
Mis VK-CPK83-USA
FDA UDI
Class IIUnknown
Mis MM-OUP01
FDA UDI
Class IUnknown
Mis MK-CPK41
FDA UDI
Class IIActive
Mis VS-P6255
FDA UDI
Class IIActive
Mis Seven MF7-13375
FDA UDI
Class IIActive
MIS Equator CK-NOE1
FDA UDI
Class IIActive
Mis CW-TCI13
FDA UDI
Class IIActive
Mis CN-LOC03
FDA UDI
Class IIActive
MIS Multi Unit MA-SA301
FDA UDI
Class IIActive
Mis VS-P6355
FDA UDI
Class IIActive
Mis MH-53330
FDA UDI
Class IIActive
Mis CW-HS550
FDA UDI
Class IIActive
Mis LC3-00315
FDA UDI
Class IIActive
Mis MD-LOC03
FDA UDI
Class IIActive
Mis CT-TDC40
FDA UDI
Class IActive
Mis MK-WLC5
FDA UDI
Class IIActive
Mis MW-CHC55
FDA UDI
Class IIActive
Mis EK-WPK63
FDA UDI
Class IIUnknown
Mis LC3-00277
FDA UDI
Class IIActive
Mis MT-MFXGS
FDA UDI
Class IActive
Mis CG-N1639
FDA UDI
Class IActive
MIS Ball Attachment MB-N4375
FDA UDI
Class IIActive
Mis LNXC-16330
FDA UDI
Class IIActive
Mis C1C-10375
FDA UDI
Class IIActive
Mis MF5-16420
FDA UDI
Class IIActive
Mis CS-C3057
FDA UDI
Class IIActive
Mis CW-HS455
FDA UDI
Class IIActive
Mis EK-CPK41
FDA UDI
Class IIUnknown

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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