← Back to catalogue

Invisible Retainer

FDA UDI

Class I (US FDA UDI)

by Allesee Aoa-Pro

Identity

Trade Name
Invisible Retainer FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Device Name
Invisible Retainer FDA UDI
Model / Reference
3000-0003 FDA UDI
Description
Invisible Retainer FDA UDI

Identifiers

Primary DI / UDI-DI
00889989038415 FDA UDI
FDA Product Code
DYJ FDA UDI
GMDN Term
Orthodontic retainer 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic retainer

Invisible Retainer by Allesee Aoa-Pro — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Allesee Aoa-Pro

Sources (1)

  • FDA UDI c90c1a29-b3e4-4046-91c3-32c733408a38 34 fields · synced May 30, 2026