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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 39 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MG-ND01
FDA UDI
Class IActive
Mis MD-FTB30
FDA UDI
Class IIActive
Mis CS-LOC03
FDA UDI
Class IIActive
Mis VN-TPA10
FDA UDI
Class IIActive
Mis MA-SO171
FDA UDI
Class IIActive
Mis CN-CPK61
FDA UDI
Class IIActive
Mis CS-HA475
FDA UDI
Class IIActive
Mis EH-06410
FDA UDI
Class IIActive
MIS Multi Unit MA-S2480
FDA UDI
Class IIActive
Mis CK-SPS55
FDA UDI
Class IIActive
Mis M7C-18420
FDA UDI
Class IIActive
Mis MB-PPR10
FDA UDI
Class IActive
Mis C1C-11500
FDA UDI
Class IIActive
Mis CN-MAB10
FDA UDI
Class IActive
Mis ED-CPK63
FDA UDI
Class IIUnknown
MIS Equator CS-OE237
FDA UDI
Class IIUnknown
Mis MT-TDN38
FDA UDI
Class IActive
Mis CS-HS348
FDA UDI
Class IIActive
Mis 4bone 4B-S3040
FDA UDI
Class IIActive
Mis MW-WMAC1
FDA UDI
Class IIActive
Mis MF7-D13420
FDA UDI
Class IIActive
Mis 4bone 4B-S2030
FDA UDI
Class IIActive
Mis CK-WPK83
FDA UDI
Class IIUnknown
Mis CK-CPK82-USA
FDA UDI
Class IIUnknown
Mis MN-RSM10
FDA UDI
Class IActive
Mis MD-A0010
FDA UDI
Class IIActive
Mis MK-0045
FDA UDI
Class IActive
Mis VN-TCI13
FDA UDI
Class IIActive
Mis MG-N1024
FDA UDI
Class IActive
Mis MK-BS001
FDA UDI
Class IActive
MIS Multi Unit CM-WA174
FDA UDI
Class IIActive
Mis MG-D1624
FDA UDI
Class IActive
MIS Ball Attachment MB-N3375
FDA UDI
Class IIActive
MIS Equator ED-OE441
FDA UDI
Class IIUnknown
Mis EW-P0010
FDA UDI
Class IIUnknown
Mis CS-CPK62
FDA UDI
Class IIActive
Mis MG-NTAS0
FDA UDI
Class IActive
Mis MK-0016
FDA UDI
Class IActive
Mis MT-BTL36
FDA UDI
Class IActive
Mis MK-WPK82
FDA UDI
Class IIActive
Mis MN-E0160
FDA UDI
Class IIActive
Mis CF5-10420
FDA UDI
Class IIActive
Mis MF7-D11330
FDA UDI
Class IIActive
Mis MG-LS041
FDA UDI
Class IActive
Mis EC1-00410
FDA UDI
Class IIActive
Mis CS-TB015
FDA UDI
Class IIActive
Mis CW-HA450
FDA UDI
Class IIActive
Mis MT-BTT55
FDA UDI
Class IActive
Mis CG-D1133
FDA UDI
Class IActive
Mis MK-CPK61
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