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Mis

FDA UDI

Class II (US FDA UDI)

by MIS Implants Technologies Ltd.

Identity

Trade Name
MIS FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
CONNECT Ø5.7, free rotation temporary cylinder FDA UDI
Model / Reference
MM-TC057 FDA UDI
Description
CONNECT Ø5.7, free rotation temporary cylinder FDA UDI

Identifiers

Catalog Number
MM-TC057 FDA UDI
Primary DI / UDI-DI
07290113991057 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

Mis by MIS Implants Technologies Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 768e613e-9035-4df2-bb96-a8766f435cac 34 fields · synced Jun 8, 2026