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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 28 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MD-CP050
FDA UDI
Class IIActive
MIS Multi Unit CM-S5480
FDA UDI
Class IIActive
Mis MK-SLC2
FDA UDI
Class IIActive
Mis MN-CHC40
FDA UDI
Class IIUnknown
Mis EH-05410
FDA UDI
Class IIActive
Mis MK-CPK81
FDA UDI
Class IIActive
Mis CF5C-16330
FDA UDI
Class IIActive
MIS Multi Unit CM-SA304
FDA UDI
Class IIActive
Mis MG-N1337
FDA UDI
Class IActive
Mis MF5-16500
FDA UDI
Class IIActive
Mis Mistral MF9-16375
FDA UDI
Class IIActive
Mis MT-ETD32
FDA UDI
Class IActive
Mis MK-WPK83
FDA UDI
Class IIActive
Mis MW-MAC10
FDA UDI
Class IIActive
Mis MW-MAB10
FDA UDI
Class IActive
Mis MU-I0480
FDA UDI
Class IActive
Mis MT-RE160
FDA UDI
Class IActive
Mis CF5-10330
FDA UDI
Class IIActive
Mis V3C-16500
FDA UDI
Class IIActive
Mis VN-IN060
FDA UDI
Class IIActive
Mis M7C-13420
FDA UDI
Class IIActive
MIS Multi Unit MA-W1500
FDA UDI
Class IIUnknown
Mis EH-W3630
FDA UDI
Class IIActive
Mis CF5-11420
FDA UDI
Class IIActive
Mis CS-CPK61
FDA UDI
Class IIActive
Mis CW-HS355
FDA UDI
Class IIActive
Mis EK-CPK43
FDA UDI
Class IIActive
Mis MT-SCD20
FDA UDI
Class IActive
Mis MT-LM005
FDA UDI
Class IActive
Mis MB-SF200
FDA UDI
Class IActive
Mis MK-CPK64
FDA UDI
Class IIActive
Mis MW-PF550
FDA UDI
Class IActive
Mis Seven MF7-11600
FDA UDI
Class IIActive
Mis M7C-06420
FDA UDI
Class IIActive
Mis CF5-13330
FDA UDI
Class IIActive
Mis MD-G0213
FDA UDI
Class IActive
Mis MM-BLA10
FDA UDI
Class IActive
Mis MH-W5500
FDA UDI
Class IIActive
Mis CK-NPK63
FDA UDI
Class IIActive
Mis MK-SVXD
FDA UDI
Class IActive
Mis MF7-18375
FDA UDI
Class IIActive
Mis MN-CPK43
FDA UDI
Class IIUnknown
Mis M5C-11330
FDA UDI
Class IIActive
Mis LNXC-11500
FDA UDI
Class IIActive
MIS Ball Attachment EW-B1550
FDA UDI
Class IIUnknown
Mis MC1-00330
FDA UDI
Class IIActive
Mis CS-IC485
FDA UDI
Class IActive
Mis MT-RT001
FDA UDI
Class IActive
Mis CG-N0833
FDA UDI
Class IActive
Mis MK-BC101
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