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 15 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis C1-D10330
FDA UDI
Class IIActive
Mis CW-RSM10
FDA UDI
Class IActive
Mis CW-AT002
FDA UDI
Class IIActive
Mis VN-AT101
FDA UDI
Class IIActive
MIS Multi Unit MA-S5480
FDA UDI
Class IIActive
Mis 4bone 4B-X2540
FDA UDI
Class IIActive
Mis MM-IO040
FDA UDI
Class IActive
Mis MT-UML21
FDA UDI
Class IUnknown
Mis MD-MACF1
FDA UDI
Class IIActive
Mis CS-CPK44
FDA UDI
Class IIActive
Mis MM-IC057
FDA UDI
Class IActive
MIS Multi Unit CM-WA171
FDA UDI
Class IIActive
Mis CS-H0843
FDA UDI
Class IIActive
Mis CN-CPK41
FDA UDI
Class IIActive
Mis V3-08390
FDA UDI
Class IIActive
MIS Equator CK-NOE3
FDA UDI
Class IIActive
Mis MG-D0637
FDA UDI
Class IActive
Mis C1-D11375
FDA UDI
Class IIActive
Mis MK-NPK63
FDA UDI
Class IIActive
Mis MT-TDI50
FDA UDI
Class IActive
Mis MT-CLR21
FDA UDI
Class IActive
Mis CN-LOC05
FDA UDI
Class IIActive
Mis MT-PP001
FDA UDI
Class IUnknown
Mis MA-SC448
FDA UDI
Class IIActive
Mis VN-IN160
FDA UDI
Class IIActive
Mis MN-TBC15
FDA UDI
Class IIActive
Mis ED-CP013
FDA UDI
Class IIUnknown
MIS Equator CW-OE350
FDA UDI
Class IIUnknown
Mis MA-WO173
FDA UDI
Class IIActive
Mis CD-AN015
FDA UDI
Class IIActive
Mis VG-NRN10
FDA UDI
Class IActive
Mis VK-CPK84-USA
FDA UDI
Class IIUnknown
Mis CF5C-10330
FDA UDI
Class IIActive
Mis MF5-10330
FDA UDI
Class IIActive
Mis MK-SLC4
FDA UDI
Class IIActive
Mis VS-TC033
FDA UDI
Class IIActive
Mis MT-BTT24
FDA UDI
Class IActive
Mis CS-TC023
FDA UDI
Class IIActive
Mis MA-WC348
FDA UDI
Class IIActive
Mis MK-CPK62
FDA UDI
Class IIActive
Mis CD-SA700
FDA UDI
Class IIActive
Mis MB-NR025
FDA UDI
Class IIUnknown
Mis CN-HS540
FDA UDI
Class IIActive
Mis M4 MF4-08500
FDA UDI
Class IIActive
Mis EK-WPK83
FDA UDI
Class IIUnknown
Mis V3-16330
FDA UDI
Class IIActive
Mis CF5-16330
FDA UDI
Class IIActive
Mis MH-55375
FDA UDI
Class IIActive
Mis CG-D1650
FDA UDI
Class IActive
Mis MW-FTB15
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