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Crozat - Lower

FDA UDI

Class I (US FDA UDI)

by Five Star Orthodontic Laboratory & Supply, Inc.

Identity

Trade Name
Crozat - Lower FDA UDI
Generic Name
Orthodontic palate expander/teeth aligner, self-removable FDA UDI
Model / Reference
5000280 FDA UDI

Identifiers

Primary DI / UDI-DI
D82850002800 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Orthodontic palate expander/teeth aligner, self-removable 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: Orthodontic palate expander/teeth aligner, self-removable

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

Similar devices

Also classified as Orthodontic palate expander/teeth aligner, self-removable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b3427a6a-0d4f-424a-8b71-88d5bc708e3e 32 fields · synced Jun 1, 2026