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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
—
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 14 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CT-NSR30
FDA UDI
Class IActive
Mis CG-TAS55
FDA UDI
Class IActive
Mis CT-BTC30
FDA UDI
Class IActive
Mis MN-IC040
FDA UDI
Class IActive
Mis MN-CPH13
FDA UDI
Class IIActive
Mis MO1-RSA10
FDA UDI
Class IUnknown
Mis CW-AN151
FDA UDI
Class IIActive
MIS Multi Unit MA-SA171
FDA UDI
Class IIActive
Mis MH-56330
FDA UDI
Class IIActive
Mis CT-TDC30
FDA UDI
Class IActive
Mis Mistral MF9-13410
FDA UDI
Class IIActive
MIS BondBone BS-BBSMP
FDA UDI
Class IIActive
MIS Ball Attachment MW-B5500
FDA UDI
Class IIActive
Mis CN-TBF15
FDA UDI
Class IIActive
MIS Locator MB-WZL06
FDA UDI
Class IIActive
Mis MN-GPC10
FDA UDI
Class IIActive
MIS Multi Unit MA-S1375
FDA UDI
Class IIUnknown
Mis MM-LRM10
FDA UDI
Class IIUnknown
Mis MA-SO303
FDA UDI
Class IIActive
Mis ED-PF410
FDA UDI
Class IUnknown
MIS Equator MK-WOE3
FDA UDI
Class IIActive
Mis CF5C-08500
FDA UDI
Class IIActive
Mis CS-B2375
FDA UDI
Class IIActive
Mis MN-CPK64
FDA UDI
Class IIUnknown
Mis MF7-D11500
FDA UDI
Class IIActive
Mis C1-D11420
FDA UDI
Class IIActive
Mis MH-04375
FDA UDI
Class IIActive
Mis MT-ELR10
FDA UDI
Class IActive
Mis VN-MAB10
FDA UDI
Class IActive
Mis MT-HHR07
FDA UDI
Class IUnknown
Mis MT-LBT24
FDA UDI
Class IActive
Mis MD-CPK64
FDA UDI
Class IIUnknown
Mis MG-D1142
FDA UDI
Class IActive
Mis MB-PR010
FDA UDI
Class IActive
Mis Mistral MF9-13480
FDA UDI
Class IIUnknown
MIS Equator CK-SOE4
FDA UDI
Class IIActive
Mis MM-GRU10
FDA UDI
Class IIUnknown
Mis MN-GP010
FDA UDI
Class IIActive
MIS Ball Attachment MB-N5375
FDA UDI
Class IIActive
Mis MH-05375
FDA UDI
Class IIActive
Mis MT-TDN20
FDA UDI
Class IUnknown
Mis EW-CPK62
FDA UDI
Class IIUnknown
Mis CK-WPC4
FDA UDI
Class IIUnknown
MIS Equator EK-SOE5
FDA UDI
Class IIUnknown
Mis C1 C1-16500
FDA UDI
Class IIActive
Mis M7C-10420
FDA UDI
Class IIActive
Mis MT-CS410
FDA UDI
Class IActive
Mis CG-D0833
FDA UDI
Class IActive
Mis MT-RSM30
FDA UDI
Class IActive
Mis MM-IOI11
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