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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 6 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MA-SC248
FDA UDI
Class IIActive
MIS Ball Attachment MB-N2375
FDA UDI
Class IIActive
Mis MU-TO480
FDA UDI
Class IIActive
Mis MT-S5010
FDA UDI
Class IUnknown
Mis V3C-13430
FDA UDI
Class IIActive
Mis MN-IT100
FDA UDI
Class IActive
Mis MH-54375
FDA UDI
Class IIActive
Mis Seven MF7-10330
FDA UDI
Class IIActive
Mis MD-ICH40
FDA UDI
Class IActive
Mis MW-RSM40
FDA UDI
Class IActive
MIS Locator MB-WZL01
FDA UDI
Class IIUnknown
Mis ED-A1510
FDA UDI
Class IIUnknown
Mis MA-NO171
FDA UDI
Class IIActive
Mis CG-D1043
FDA UDI
Class IActive
Mis ED-CPK84
FDA UDI
Class IIActive
MIS Multi Unit CS-S1375
FDA UDI
Class IIUnknown
Mis MM-LOA40
FDA UDI
Class IActive
Mis VS-P6455
FDA UDI
Class IIActive
Mis MD-RSM80
FDA UDI
Class IActive
Mis Seven MF7-16375
FDA UDI
Class IIActive
Mis MM-PC100
FDA UDI
Class IActive
Mis MN-CP013
FDA UDI
Class IIActive
Mis VN-P4240
FDA UDI
Class IIActive
Mis MK-NLC5
FDA UDI
Class IIActive
Mis MH-N2330
FDA UDI
Class IIActive
MIS Multi Unit CS-S3375
FDA UDI
Class IIUnknown
Mis MM-TCI57
FDA UDI
Class IIActive
Mis MT-S4511
FDA UDI
Class IActive
Mis MT-RB225
FDA UDI
Class IActive
Mis MF7-D08420
FDA UDI
Class IIActive
Mis CG-N1333
FDA UDI
Class IActive
Mis V3C-10390
FDA UDI
Class IIActive
Mis MM-RSM57
FDA UDI
Class IActive
Mis MT-CSM21
FDA UDI
Class IActive
Mis CK-SIC6
FDA UDI
Class IIUnknown
Mis MT-RKS15
FDA UDI
Class IUnknown
Mis CG-GMW10
FDA UDI
Class IActive
Mis CT-P2408
FDA UDI
Class IActive
Mis MT-ETD28
FDA UDI
Class IActive
Mis Mistral MF9-08480
FDA UDI
Class IIActive
Mis MT-BT032
FDA UDI
Class IActive
Mis CT-NLI10
FDA UDI
Class IActive
Mis M5C-13330
FDA UDI
Class IIActive
Mis VS-AT153
FDA UDI
Class IIActive
Mis MK-0057
FDA UDI
Class IActive
Mis MG-KD01
FDA UDI
Class IActive
Mis MT-TDT45
FDA UDI
Class IActive
Mis MM-CC040
FDA UDI
Class IIUnknown
Mis VK-NPK63
FDA UDI
Class IIActive
Mis MG-D1642
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