Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
514576057

Catalogue (2090)

Page 9 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CK-SPS70
FDA UDI
Class IIUnknown
Mis MD-MAB10
FDA UDI
Class IActive
Mis MU-IT480
FDA UDI
Class IActive
Mis CS-A1510
FDA UDI
Class IIActive
Mis MW-CHC80
FDA UDI
Class IIUnknown
Mis MF5-13375
FDA UDI
Class IIActive
Mis MT-BTT38
FDA UDI
Class IActive
Mis C1 C1-08420
FDA UDI
Class IIActive
Mis MK-WPZ4
FDA UDI
Class IIUnknown
Mis MW-CHC60
FDA UDI
Class IIUnknown
Mis EW-GPC10
FDA UDI
Class IIActive
Mis CK-WLC1
FDA UDI
Class IIActive
Mis MW-TPH50
FDA UDI
Class IIActive
Mis CK-CPK63
FDA UDI
Class IIActive
Mis CS-IO485
FDA UDI
Class IActive
MIS Equator MD-OE437
FDA UDI
Class IIUnknown
Mis MF7-D13330
FDA UDI
Class IIActive
Mis MT-GDN50
FDA UDI
Class IActive
Mis LNXC-11420
FDA UDI
Class IIActive
Mis MK-0059
FDA UDI
Class IActive
Mis CF5C-13375
FDA UDI
Class IIActive
Mis MM-IO450
FDA UDI
Class IUnknown
MIS Ball Attachment MW-B1500
FDA UDI
Class IIActive
Mis M7C-11420
FDA UDI
Class IIActive
Mis MW-ITC30
FDA UDI
Class IActive
Mis MW-GPCG1
FDA UDI
Class IIUnknown
Mis MG-D0633
FDA UDI
Class IActive
MIS Multi Unit CM-N1480
FDA UDI
Class IIActive
Mis MD-TCH23
FDA UDI
Class IIActive
Mis MF7-D11420
FDA UDI
Class IIActive
Mis LT-SLM10
FDA UDI
Class IActive
Mis CW-MC103
FDA UDI
Class IIActive
Mis CS-CPK83
FDA UDI
Class IIActive
Mis Lance EF5-10375
FDA UDI
Class IIActive
Mis ED-A0010
FDA UDI
Class IIUnknown
Mis C1C-16500
FDA UDI
Class IIActive
Mis VK-NIC6
FDA UDI
Class IIUnknown
Mis M5C-10600
FDA UDI
Class IIActive
Mis MM-CHC40
FDA UDI
Class IIUnknown
Mis VS-HS458
FDA UDI
Class IIActive
Mis MN-RSM40
FDA UDI
Class IActive
Mis M5C-10420
FDA UDI
Class IIActive
Mis CN-AT202
FDA UDI
Class IIActive
Mis CN-HA248
FDA UDI
Class IIActive
Mis CS-PF375
FDA UDI
Class IActive
Mis MH-N3330
FDA UDI
Class IIActive
Mis MG-DLG55
FDA UDI
Class IActive
Mis MH-S0448
FDA UDI
Class IIActive
Mis LNXC-10500
FDA UDI
Class IIActive
Mis CS-TPH50
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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