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Mis

FDA UDI

Class I (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
LOCKiT analog Ø5 mm, WP FDA UDI
Model / Reference
MM-LOA50 FDA UDI
Description
LOCKiT analog Ø5 mm, WP FDA UDI

Identifiers

Catalog Number
MM-LOA50 FDA UDI
Primary DI / UDI-DI
07290109010182 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

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 Dental Implant Suprastructure, Temporary - a single-use preformed device intended for use during dental implant restorative and laboratory procedures. It provides a temporary intermediate fixture level between a dental implant and a temporary prosthesis/restoration during the oral soft-tissue healing and sculpturing period.

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

Manufacturer
MIS Implants Technologies Ltd.

Sources (1)

  • FDA UDI 3a033df0-34b0-49cf-af78-c14b4e5dea21 34 fields · synced Jul 26, 2026