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 34 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MD-A2510
FDA UDI
Class IIActive
Mis MT-TF172
FDA UDI
Class IActive
Mis CW-C2040
FDA UDI
Class IIActive
Mis CW-CPK64
FDA UDI
Class IIActive
Mis MA-WO171
FDA UDI
Class IIActive
Mis MT-HKL21
FDA UDI
Class IUnknown
Mis MK-SDS06
FDA UDI
Class IActive
Mis MF5-11330
FDA UDI
Class IIActive
Mis MW-IT340
FDA UDI
Class IActive
Mis MT-BTI20
FDA UDI
Class IActive
Mis MK-WPK43
FDA UDI
Class IIActive
Mis MU-RSM48
FDA UDI
Class IActive
Mis CW-TB001
FDA UDI
Class IIActive
Mis MW-CPH60
FDA UDI
Class IIActive
Mis CT-WLR10
FDA UDI
Class IActive
Mis MD-TBC15
FDA UDI
Class IIActive
Mis MT-TDT38
FDA UDI
Class IActive
Mis MD-CPC64
FDA UDI
Class IIActive
Mis M7C-13330
FDA UDI
Class IIActive
Mis MD-FTB15
FDA UDI
Class IIActive
Mis MN-CHC60
FDA UDI
Class IIUnknown
Mis OE-RSM60
FDA UDI
Class IActive
Mis MW-ICH40
FDA UDI
Class IActive
Mis CT-SSM30
FDA UDI
Class IActive
Mis CF5-08420
FDA UDI
Class IIActive
Mis C1 C1-13375
FDA UDI
Class IIActive
Mis VS-P8455
FDA UDI
Class IIActive
Mis MT-S2011
FDA UDI
Class IUnknown
Mis CG-N1039
FDA UDI
Class IActive
Mis MD-LOC01
FDA UDI
Class IIActive
Mis CW-TCI33
FDA UDI
Class IIActive
MIS Locator MB-WZL02
FDA UDI
Class IIUnknown
Mis M7C-13375
FDA UDI
Class IIActive
Mis MK-CCLAS
FDA UDI
Class IIActive
Mis MT-RDE30
FDA UDI
Class IActive
Mis Lance EF5-08500
FDA UDI
Class IIActive
Mis MF7-D13375
FDA UDI
Class IIActive
Mis CG-D1643
FDA UDI
Class IActive
Mis MD-CPK84
FDA UDI
Class IIUnknown
MIS Equator CK-SOE2
FDA UDI
Class IIActive
Mis CT-BGP46
FDA UDI
Class IUnknown
Mis 4bone 4B-P0010
FDA UDI
UActive
Mis CK-NPK43
FDA UDI
Class IIActive
Mis CS-HS648
FDA UDI
Class IIActive
Mis CN-MAN10
FDA UDI
Class IActive
Mis MK-0014
FDA UDI
Class IUnknown
Mis MN-LOC02
FDA UDI
Class IIActive
Mis MG-TMP50
FDA UDI
Class IActive
Mis CW-LOC05
FDA UDI
Class IIActive
Mis MD-E0220
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