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Twin Block

FDA UDI

Class I (US FDA UDI)

by Five Star Orthodontic Laboratory & Supply, Inc.

Identity

Trade Name
Twin Block FDA UDI
Generic Name
Removable dental occlusal splint, custom-made FDA UDI
Model / Reference
5000190 FDA UDI

Identifiers

Primary DI / UDI-DI
D82850001900 FDA UDI
FDA Product Code
DYJ FDA UDI
GMDN Term
Removable dental occlusal splint, custom-made FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 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

Yes

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

Yes

FDA UDI

Category: Removable dental occlusal splint, custom-made

Twin Block by Five Star Orthodontic Laboratory & Supply, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Removable dental occlusal splint, custom-made.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 54f62806-b2d2-47b3-a9df-b1f416d7479a 32 fields · synced May 30, 2026