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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 2 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MK-0021
FDA UDI
Class IUnknown
Mis EH-54410
FDA UDI
Class IIActive
Mis Provisional Implant TF1-B1024
FDA UDI
Class IIActive
Mis CG-N1339
FDA UDI
Class IActive
Mis MT-SRH20
FDA UDI
Class IActive
Mis VK-CPK63
FDA UDI
Class IIActive
Mis VK-CPK62
FDA UDI
Class IIActive
Mis VN-P6440
FDA UDI
Class IIActive
Mis CS-LOC01
FDA UDI
Class IIActive
Mis MW-TBC30
FDA UDI
Class IIActive
Mis MD-CTP10
FDA UDI
Class IIActive
Mis VS-HS658
FDA UDI
Class IIActive
Mis ED-GP100
FDA UDI
Class IUnknown
Mis V3-11500
FDA UDI
Class IIActive
Mis MG-D0642
FDA UDI
Class IActive
Mis CW-C3040
FDA UDI
Class IIActive
Mis MT-TD350
FDA UDI
Class IUnknown
Mis CN-C2040
FDA UDI
Class IIActive
Mis MT-ESR10
FDA UDI
Class IActive
Mis CF5C-13500
FDA UDI
Class IIActive
Mis M5C-13375
FDA UDI
Class IIActive
Mis 4bone 4B-C1520
FDA UDI
Class IIActive
Mis M7C-10600
FDA UDI
Class IIActive
Mis Ortho Anchor Screw MG2-12160
FDA UDI
Class IIActive
Mis MG-N1037
FDA UDI
Class IActive
Mis Seven MF7-11375
FDA UDI
Class IIActive
Mis LT-SLR10
FDA UDI
Class IActive
Mis CW-GPC10
FDA UDI
Class IIActive
Mis MA-WO301
FDA UDI
Class IIActive
Mis MT-S3011
FDA UDI
Class IUnknown
Mis MH-N0540
FDA UDI
Class IIActive
MIS Equator CK-SOE5
FDA UDI
Class IIActive
Mis MD-SP102
FDA UDI
Class IActive
Mis CT-P2413
FDA UDI
Class IActive
Mis CW-LOC01
FDA UDI
Class IIActive
Mis CN-TPH50
FDA UDI
Class IIActive
Mis LNXC-16500
FDA UDI
Class IIActive
Mis MK-SDS10
FDA UDI
Class IActive
Mis MD-AN250
FDA UDI
Class IIUnknown
MIS Ball Attachment MB-N4330
FDA UDI
Class IIActive
Mis CS-H0439
FDA UDI
Class IIActive
Mis CS-C2057
FDA UDI
Class IIActive
Mis MD-GPC10
FDA UDI
Class IIActive
Mis MD-TPA12
FDA UDI
Class IIActive
MIS Multi Unit CS-S2375
FDA UDI
Class IIActive
Mis MK-CPC64
FDA UDI
Class IIActive
Mis CG-D1343
FDA UDI
Class IActive
Mis MT-CD490
FDA UDI
Class IActive
Mis CW-TB030
FDA UDI
Class IIActive
Mis ED-AN151
FDA UDI
Class IIUnknown

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