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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
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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 1 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CG-N1633
FDA UDI
Class IActive
Mis MT-PP240
FDA UDI
Class IActive
MIS Equator MK-WOE1
FDA UDI
Class IIActive
Mis MM-CHC55
FDA UDI
Class IIUnknown
Mis MD-LOC04
FDA UDI
Class IIActive
Mis MW-CPH13
FDA UDI
Class IIActive
Mis CG-D1050
FDA UDI
Class IActive
Mis MT-P2406
FDA UDI
Class IUnknown
Mis MK-NPK41
FDA UDI
Class IIActive
Mis CF5C-10420
FDA UDI
Class IIActive
Mis LT-WSR10
FDA UDI
Class IActive
Mis ED-DI001
FDA UDI
Class IUnknown
Mis MK-CPK82
FDA UDI
Class IIActive
Mis CW-CPK62
FDA UDI
Class IIActive
Mis CS-AN251
FDA UDI
Class IIActive
MIS BondBone BS-BB005
FDA UDI
Class IIActive
Mis MG-IE160
FDA UDI
Class IActive
Mis EW-TPH50
FDA UDI
Class IIActive
Mis CM-NO172
FDA UDI
Class IIActive
Mis VN-TCI33
FDA UDI
Class IIActive
Mis MG-PTAS0
FDA UDI
Class IActive
Mis MK-C101
FDA UDI
Class IActive
Mis CS-H0443
FDA UDI
Class IIActive
Mis Ortho Anchor Screw MG2-06160
FDA UDI
Class IIActive
Mis CM-WO171
FDA UDI
Class IIActive
Mis CS-A2510
FDA UDI
Class IIActive
Mis CS-IT300
FDA UDI
Class IActive
Mis CG-GRN10
FDA UDI
Class IActive
Mis CS-TB002
FDA UDI
Class IIActive
Mis C1-D16420
FDA UDI
Class IIActive
Mis CT-BTC40
FDA UDI
Class IActive
Mis CK-NLC1
FDA UDI
Class IIActive
Mis MT-SRA10
FDA UDI
Class IActive
Mis MT-CS375
FDA UDI
Class IActive
Mis Mistral MF9-10410
FDA UDI
Class IIActive
Mis MW-TC033
FDA UDI
Class IIActive
Mis CW-AT003
FDA UDI
Class IIActive
Mis CN-TCI23
FDA UDI
Class IIActive
Mis M5C-13500
FDA UDI
Class IIActive
Mis Mistral MF9-10375
FDA UDI
Class IIActive
MIS Ti Base MD-TB002
FDA UDI
Class IIActive
Mis MM-CEI46
FDA UDI
Class IIActive
Mis CK-CPK62
FDA UDI
Class IIActive
Mis MK-SDS11
FDA UDI
Class IActive
Mis MF7-D11375
FDA UDI
Class IIActive
Mis CS-I0375
FDA UDI
Class IActive
Mis MN-IT340
FDA UDI
Class IActive
Mis CW-CPK61
FDA UDI
Class IIActive
Mis VG-GMN10
FDA UDI
Class IActive
Mis VK-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