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Positioner (Standard Set-Up)

FDA UDI

Class I (US FDA UDI)

by Five Star Orthodontic Laboratory & Supply, Inc.

Identity

Trade Name
Positioner (Standard Set-Up) FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Model / Reference
5200130 FDA UDI

Identifiers

Primary DI / UDI-DI
D82852001300 FDA UDI
FDA Product Code
KMY FDA UDI
GMDN Term
Orthodontic retainer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5525 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 retainer

Positioner (Standard Set-Up) 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 retainer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4ad0c804-8909-4874-89ca-10377ede6ed2 32 fields · synced May 30, 2026