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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 23 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis M4 MF4-06500
FDA UDI
Class IIActive
Mis CK-CPK64-USA
FDA UDI
Class IIActive
Mis MM-MAN57
FDA UDI
Class IActive
Mis C1C-10330
FDA UDI
Class IIActive
Mis VN-P4440
FDA UDI
Class IIActive
Mis MW-CP013
FDA UDI
Class IIActive
Mis EK-WPK41
FDA UDI
Class IIUnknown
Mis CD-CM488
FDA UDI
Class IIUnknown
Mis CS-IT340
FDA UDI
Class IActive
Mis MT-CD365
FDA UDI
Class IActive
Mis MK-0040
FDA UDI
Class IUnknown
Mis 4matrix BS-4MXSP
FDA UDI
Class IIActive
Mis MK-WPK63
FDA UDI
Class IIActive
Mis MT-ESM10
FDA UDI
Class IActive
Mis 4bone 4B-C3040
FDA UDI
Class IIActive
MIS Equator CS-OE537
FDA UDI
Class IIUnknown
Mis V3C-11330
FDA UDI
Class IIActive
Mis Lance EF5-08420
FDA UDI
Class IIActive
Mis CH-15550
FDA UDI
Class IIActive
Mis CD-AN020
FDA UDI
Class IIUnknown
Mis MM-RED10
FDA UDI
Class IActive
MIS Ball Attachment MB-AN252
FDA UDI
Class IIActive
Mis V3C-11430
FDA UDI
Class IIActive
Mis MT-BT055
FDA UDI
Class IActive
Mis Lance EF5-13375
FDA UDI
Class IIActive
Mis MW-TCH13
FDA UDI
Class IIActive
Mis CK-NPK61
FDA UDI
Class IIActive
Mis MD-CPK61
FDA UDI
Class IIUnknown
Mis MT-RSD24
FDA UDI
Class IActive
Mis CT-NSI10
FDA UDI
Class IActive
Mis MN-CPK61
FDA UDI
Class IIUnknown
Mis MG-D1337
FDA UDI
Class IActive
Mis M5C-16330
FDA UDI
Class IIActive
Mis CG-N1033
FDA UDI
Class IActive
Mis CK-CPK42
FDA UDI
Class IIActive
Mis M4 MF4-10600
FDA UDI
Class IIActive
Mis CF5-10500
FDA UDI
Class IIActive
Mis MG-N0824
FDA UDI
Class IActive
Mis C1C-08420
FDA UDI
Class IIActive
Mis CS-AN151
FDA UDI
Class IIActive
Mis CN-H0833
FDA UDI
Class IIActive
Mis CW-AT252
FDA UDI
Class IIActive
Mis CS-A0010
FDA UDI
Class IIActive
Mis CG-N1133
FDA UDI
Class IActive
Mis VS-AT252
FDA UDI
Class IIActive
Mis CT-BTC24
FDA UDI
Class IActive
Mis MT-S3211
FDA UDI
Class IActive
Mis VK-CPK63-USA
FDA UDI
Class IIUnknown
Mis VK-NPK63-USA
FDA UDI
Class IIActive
Mis MT-RE172
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