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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
—
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 33 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CS-A0030
FDA UDI
Class IIActive
Mis MM-CF048
FDA UDI
Class IIActive
Mis MT-00500
FDA UDI
Class IActive
Mis MT-CD310
FDA UDI
Class IActive
Mis MK-CPC63
FDA UDI
Class IIActive
Mis CK-CPK44
FDA UDI
Class IIActive
Mis MW-RSM10
FDA UDI
Class IActive
Mis MF5-11600
FDA UDI
Class IIActive
Mis ED-IT300
FDA UDI
Class IUnknown
Mis MT-P2413
FDA UDI
Class IUnknown
Mis MM-CE046
FDA UDI
Class IIActive
Mis MM-LMP10
FDA UDI
Class IIUnknown
Mis CW-I0500
FDA UDI
Class IActive
Mis MN-GP100
FDA UDI
Class IActive
Mis M5C-08420
FDA UDI
Class IIActive
MIS Ti Base MN-TB002
FDA UDI
Class IIActive
Mis ED-GPC10
FDA UDI
Class IIActive
Mis MG-N0837
FDA UDI
Class IActive
Mis CT-NLR30
FDA UDI
Class IActive
Mis MD-LOC05
FDA UDI
Class IIActive
Mis MM-LOA50
FDA UDI
Class IActive
Mis EW-I0500
FDA UDI
Class IUnknown
Mis MG-FS020
FDA UDI
Class IActive
Mis MN-CPK41
FDA UDI
Class IIUnknown
Mis OE-RCB01
FDA UDI
Class IActive
Mis MW-MAN10
FDA UDI
Class IActive
Mis CF5C-11375
FDA UDI
Class IIActive
Mis VS-TCI13
FDA UDI
Class IIActive
Mis MB-TBS10
FDA UDI
Class IUnknown
Mis CN-HS833
FDA UDI
Class IIActive
Mis MK-WLC1
FDA UDI
Class IIActive
Mis MD-TCH13
FDA UDI
Class IIActive
Mis CN-PF330
FDA UDI
Class IActive
Mis C1-D11330
FDA UDI
Class IIActive
Mis M4 MF4-13330
FDA UDI
Class IIActive
Mis EW-CPK63
FDA UDI
Class IIActive
Mis CN-CPK42
FDA UDI
Class IIActive
Mis EK-WPK62
FDA UDI
Class IIActive
Mis EW-MAC10
FDA UDI
Class IIUnknown
MIS Ti Base MW-TB001
FDA UDI
Class IIActive
Mis MD-AN150
FDA UDI
Class IIActive
MIS Multi Unit MA-W1480
FDA UDI
Class IIActive
Mis Seven MF7-11330
FDA UDI
Class IIActive
Mis CN-HA348
FDA UDI
Class IIActive
Mis OE-RCV01
FDA UDI
Class IActive
Mis OE-RCY01
FDA UDI
Class IActive
Mis Seven MF7-11420
FDA UDI
Class IIActive
Mis CH-03550
FDA UDI
Class IIActive
Mis MD-NH142
FDA UDI
Class IIUnknown
MIS Ball Attachment CW-B3500
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