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Justi Triplex MSLV Posterior Teeth 1x8

FDA UDI

Class II (US FDA UDI)

by American Tooth Industries

Identity

Trade Name
Justi Triplex MSLV Posterior Teeth 1x8 FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
Justi Triples MSLV Posterior Hardened Plastic Teeth 1x8 FDA UDI
Model / Reference
082-51-0101 FDA UDI
Description
Justi Triples MSLV Posterior Hardened Plastic Teeth 1x8 FDA UDI

Identifiers

Catalog Number
082-51-0101 FDA UDI
Primary DI / UDI-DI
D7720825101010 FDA UDI
FDA Product Code
ELM FDA UDI
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3590 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Resin artificial teeth

Justi Triplex MSLV Posterior Teeth 1x8 by American Tooth Industries — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Resin artificial teeth.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 29a00fbc-2212-489a-a5f8-086bf7d5c777 34 fields · synced Jun 1, 2026