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The Trainer System™

FDA UDI

Class I (US FDA UDI)

by Myofunctional Research Corp. Pty. , Ltd.

Identity

Trade Name
The Trainer System™ FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Model / Reference
T4K Phase 1 FDA UDI

Identifiers

Catalog Number
T4Kc-08 FDA UDI
Primary DI / UDI-DI
19330944001923 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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic retainer

The Trainer System™ by Myofunctional Research Corp. Pty. , Ltd. — 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 ab9c536a-2d29-482d-afac-5243b9d74314 33 fields · synced May 31, 2026