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 19 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis MK-CPK83
FDA UDI
Class IIActive
Mis CA-PTC13
FDA UDI
Class IIActive
MIS Locator MB-WZL00
FDA UDI
Class IIUnknown
Mis MT-BGP37
FDA UDI
Class IUnknown
Mis MN-CCI10
FDA UDI
Class IIActive
MIS Ball Attachment EB-N5410
FDA UDI
Class IIUnknown
Mis MT-S4506
FDA UDI
Class IUnknown
MIS Equator CK-WOE1
FDA UDI
Class IIActive
Mis CC1-00500
FDA UDI
Class IIActive
Mis MT-NRH20
FDA UDI
Class IUnknown
Mis VK-NPK42-USA
FDA UDI
Class IIUnknown
Mis ED-IT100
FDA UDI
Class IUnknown
Mis MW-GP0G1
FDA UDI
Class IIUnknown
Mis CT-BTC35
FDA UDI
Class IActive
Mis MN-IC600
FDA UDI
Class IActive
Mis MH-A6375
FDA UDI
Class IIActive
Mis CS-GP010
FDA UDI
Class IIActive
Mis Seven MF7-13600
FDA UDI
Class IIActive
Mis MM-H3057
FDA UDI
Class IIActive
Mis MG-D1342
FDA UDI
Class IActive
Mis V3C-16330
FDA UDI
Class IIActive
Mis VN-TPH50
FDA UDI
Class IIActive
MIS Equator MD-OE537
FDA UDI
Class IIActive
Mis Lance EF5-13500
FDA UDI
Class IIActive
Mis EW-CPK42
FDA UDI
Class IIUnknown
Mis MT-RDM30
FDA UDI
Class IActive
Mis CT-BP320
FDA UDI
Class IUnknown
Mis CG-D1350
FDA UDI
Class IActive
Mis OE-EPC01
FDA UDI
Class IIUnknown
Mis Mistral MF9-16480
FDA UDI
Class IIActive
Mis MT-SHA10
FDA UDI
Class IActive
Mis MD-CC010
FDA UDI
Class IIActive
Mis MD-G0220
FDA UDI
Class IIActive
MIS Multi Unit MA-S3480
FDA UDI
Class IIActive
MIS Equator ED-OE241
FDA UDI
Class IIActive
Mis OE-IC002
FDA UDI
Class IActive
Mis MT-BT028
FDA UDI
Class IActive
Mis CN-HS640
FDA UDI
Class IIActive
Mis MW-TBC15
FDA UDI
Class IIActive
Mis MM-IOI57
FDA UDI
Class IActive
Mis MW-RSM48
FDA UDI
Class IUnknown
Mis MN-CPK63
FDA UDI
Class IIUnknown
Mis VS-HS358
FDA UDI
Class IIActive
Mis CM-WO173
FDA UDI
Class IIActive
Mis CS-LOC05
FDA UDI
Class IIActive
Mis EW-CP013
FDA UDI
Class IIUnknown
Mis MK-0036
FDA UDI
Class IUnknown
Mis MG-BM047
FDA UDI
Class IActive
Mis CT-SLR10
FDA UDI
Class IActive
Mis CS-B1375
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