Mis

FDA UDI

Class II (US FDA UDI)

by MIS Implants Technologies Ltd.

Identity

Trade Name: MIS FDA UDI
Generic Name: Screw endosteal dental implant, two-piece FDA UDI
Device Name: Lance internal hex. implant dia.3.30 L13mm, NP FDA UDI
Model / Reference: MF5-13330 FDA UDI
Description: Lance internal hex. implant dia.3.30 L13mm, NP FDA UDI

Identifiers

Catalog Number: MF5-13330 FDA UDI
Primary DI / UDI-DI: 07290113995710 FDA UDI
FDA Product Code: DZE FDA UDI
GMDN Term: Screw endosteal dental implant, two-piece FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.3640 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Screw endosteal dental implant, two-piece

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: MIS Implants Technologies Ltd.

Sources (1)

FDA UDI 6c8094ec-7e3f-4f0b-88a9-360b50ee43e5 34 fields · synced Jun 1, 2026