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 29 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MT-S2806
FDA UDI
Class IUnknown
Mis MG-KD07
FDA UDI
Class IActive
Mis C1-D13375
FDA UDI
Class IIActive
Mis M4 MF4-06420
FDA UDI
Class IIActive
Mis MM-RSM41
FDA UDI
Class IActive
Mis V3C-13500
FDA UDI
Class IIActive
Mis MT-RI030
FDA UDI
Class IActive
Mis MW-LOC03
FDA UDI
Class IIActive
Mis MW-CPK42
FDA UDI
Class IIActive
Mis VM-NO172
FDA UDI
Class IIActive
Mis Seven MG7-11330
FDA UDI
Class IIActive
Mis MD-TC023
FDA UDI
Class IIActive
Mis C1C-13420
FDA UDI
Class IIActive
Mis M7C-08500
FDA UDI
Class IIActive
Mis CN-H0433
FDA UDI
Class IIActive
Mis ED-CTP10
FDA UDI
Class IIUnknown
Mis EW-CPK84
FDA UDI
Class IIUnknown
MIS Multi Unit CM-S2480
FDA UDI
Class IIActive
Mis EH-W4630
FDA UDI
Class IIActive
Mis CS-HS375
FDA UDI
Class IIActive
Mis MT-MLM30
FDA UDI
Class IActive
MIS Multi Unit MA-N1480
FDA UDI
Class IIActive
Mis CS-HA575
FDA UDI
Class IIActive
Mis EK-CPK81
FDA UDI
Class IIActive
Mis MN-CPK44
FDA UDI
Class IIActive
MIS Equator ED-OE341
FDA UDI
Class IIUnknown
Mis CS-TCI23
FDA UDI
Class IIActive
Mis CT-TDC35
FDA UDI
Class IActive
Mis EK-CPK44
FDA UDI
Class IIUnknown
Mis MM-CCI40
FDA UDI
Class IIUnknown
Mis 4bone 4B-X2510
FDA UDI
Class IIActive
Mis MT-C2410
FDA UDI
Class IUnknown
MIS Equator EK-SOE3
FDA UDI
Class IIUnknown
Mis CF5C-11420
FDA UDI
Class IIActive
Mis CC1-00277
FDA UDI
Class IIActive
Mis MN-MAN10
FDA UDI
Class IActive
Mis EW-RSM10
FDA UDI
Class IUnknown
Mis MT-BT045
FDA UDI
Class IActive
Mis MN-CPC64
FDA UDI
Class IIActive
Mis MD-IT300
FDA UDI
Class IActive
Mis Lance EF5-13420
FDA UDI
Class IIActive
Mis MW-FTB30
FDA UDI
Class IIActive
Mis MD-S0224
FDA UDI
Class IIActive
MIS Ti Base MK-TBN4
FDA UDI
Class IIUnknown
Mis MT-TDT32
FDA UDI
Class IActive
Mis MM-SA160
FDA UDI
Class IIActive
Mis CT-P2406
FDA UDI
Class IActive
Mis CG-SCRW0
FDA UDI
Class IActive
Mis ED-AN251
FDA UDI
Class IIUnknown
Mis MT-GDN33
FDA UDI
Class IActive

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