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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 13 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis V3-10500
FDA UDI
Class IIActive
Mis MW-CHC40
FDA UDI
Class IIUnknown
Mis M5C-13420
FDA UDI
Class IIActive
Mis MH-06375
FDA UDI
Class IIActive
Mis CF5-16500
FDA UDI
Class IIActive
Mis MD-GP010
FDA UDI
Class IIActive
Mis MM-AN204
FDA UDI
Class IIActive
Mis MT-HLI10
FDA UDI
Class IActive
MIS Locator MB-NZL01
FDA UDI
Class IIUnknown
MIS Ball Attachment EB-N1410
FDA UDI
Class IIUnknown
Mis CN-CPK62
FDA UDI
Class IIActive
Mis MN-TC033
FDA UDI
Class IIActive
Mis V3-13330
FDA UDI
Class IIActive
Mis MU-BGC48
FDA UDI
Class IIActive
Mis MT-S3511
FDA UDI
Class IActive
Mis CW-TB015
FDA UDI
Class IIActive
Mis LNXC-08375
FDA UDI
Class IIActive
Mis CS-CPK42
FDA UDI
Class IIActive
Mis MK-WPC62
FDA UDI
Class IIActive
Mis MW-TC013
FDA UDI
Class IIActive
Mis CS-B3375
FDA UDI
Class IIActive
Mis MF7-D06500
FDA UDI
Class IIActive
Mis MF5-08500
FDA UDI
Class IIActive
MIS Ball Attachment CW-B1500
FDA UDI
Class IIActive
Mis MT-RLM30
FDA UDI
Class IActive
Mis MT-RSD19
FDA UDI
Class IActive
Mis VS-TCI33
FDA UDI
Class IIActive
MIS Ti Base MN-TB001
FDA UDI
Class IIActive
Mis MK-WPK81
FDA UDI
Class IIActive
Mis MU-H4480
FDA UDI
Class IIActive
Mis MN-CPK42
FDA UDI
Class IIUnknown
Mis VS-AT001
FDA UDI
Class IIActive
Mis EH-02410
FDA UDI
Class IIActive
Mis CT-NSR10
FDA UDI
Class IActive
Mis C1 C1-08500
FDA UDI
Class IIActive
Mis MK-C1XD
FDA UDI
Class IActive
Mis MD-IB951
FDA UDI
Class IIUnknown
Mis V3C-13390
FDA UDI
Class IIActive
Mis CS-H0643
FDA UDI
Class IIActive
Mis VN-TB001
FDA UDI
Class IIActive
Mis CS-MAC10
FDA UDI
Class IIActive
Mis VG-GRN01
FDA UDI
Class IActive
Mis MH-N0440
FDA UDI
Class IIActive
Mis CG-GRS10
FDA UDI
Class IActive
Mis 4bone 4B-S1520
FDA UDI
Class IIActive
Mis CW-IO501
FDA UDI
Class IActive
Mis VS-P8155
FDA UDI
Class IIActive
Mis MM-S0160
FDA UDI
Class IIActive
MIS Equator CK-SOE3
FDA UDI
Class IIActive
Mis MG-GMI10
FDA UDI
Class IActive

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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