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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
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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 12 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MD-CPK43
FDA UDI
Class IIActive
Mis MC1-00375
FDA UDI
Class IIActive
Mis MM-IO011
FDA UDI
Class IActive
Mis C1-D08500
FDA UDI
Class IIActive
Mis MK-WPK61
FDA UDI
Class IIActive
Mis MH-N0442
FDA UDI
Class IIActive
Mis M7C-13600
FDA UDI
Class IIActive
Mis C1-D08420
FDA UDI
Class IIActive
Mis MM-ICI57
FDA UDI
Class IActive
Mis CW-MAC10
FDA UDI
Class IIUnknown
Mis CA-PTO13
FDA UDI
Class IIActive
Mis CS-CPK82
FDA UDI
Class IIActive
Mis CN-TB001
FDA UDI
Class IIActive
Mis CW-MAN10
FDA UDI
Class IActive
Mis MB-DMH10
FDA UDI
Class IActive
Mis CT-TDC45
FDA UDI
Class IActive
Mis MK-0035
FDA UDI
Class IUnknown
Mis CW-TCI23
FDA UDI
Class IIActive
MIS Ball Attachment CN-B1330
FDA UDI
Class IIActive
Mis Ortho Anchor Screw MG2-08160
FDA UDI
Class IIActive
Mis MT-MURL2
FDA UDI
Class IActive
Mis CN-AN320
FDA UDI
Class IIActive
MIS Multi Unit MA-W5480
FDA UDI
Class IIActive
Mis Provisional Implant TF1-A1324
FDA UDI
Class IIActive
Mis MG-K001
FDA UDI
Class IActive
Mis MA-NC248
FDA UDI
Class IIActive
Mis MG-NRS01
FDA UDI
Class IActive
Mis CW-C3057
FDA UDI
Class IIActive
Mis MT-HLI21
FDA UDI
Class IActive
Mis M4 MF4-16500
FDA UDI
Class IIActive
Mis MT-SE128
FDA UDI
Class IActive
Mis MG-D1124
FDA UDI
Class IActive
Mis CW-C1557
FDA UDI
Class IIActive
Mis LNXC-10420
FDA UDI
Class IIActive
Mis CK-WPK64
FDA UDI
Class IIActive
Mis CN-AT102
FDA UDI
Class IIActive
Mis GI-SCH11
FDA UDI
Class IActive
Mis MT-S3513
FDA UDI
Class IActive
Mis LNXC-11375
FDA UDI
Class IIActive
Mis MG-P1324
FDA UDI
Class IActive
Mis CT-P2416
FDA UDI
Class IActive
Mis MG-NTAS1
FDA UDI
Class IActive
Mis MK-0020
FDA UDI
Class IActive
Mis MH-N0640
FDA UDI
Class IIActive
Mis MM-GB100
FDA UDI
Class IIUnknown
Mis MD-AT152
FDA UDI
Class IIActive
Mis CG-NRS10
FDA UDI
Class IActive
Mis MT-DE001
FDA UDI
Class IActive
Mis C1C-11375
FDA UDI
Class IIActive
Mis MM-GBU10
FDA UDI
Class IIUnknown

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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