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Clearguide Express

FDA UDI

Class II (US FDA UDI)

by Allesee Aoa-Pro

Identity

Trade Name
Clearguide Express FDA UDI
Generic Name
Orthodontic progressive aligner FDA UDI
Device Name
Set of clear plastic aligners – corrects minor to intermediate anterior malalignments of teeth FDA UDI
Model / Reference
3000-0006 FDA UDI
Description
Set of clear plastic aligners – corrects minor to intermediate anterior malalignments of teeth FDA UDI

Identifiers

Primary DI / UDI-DI
00889989061987 FDA UDI
510(k) Number
K093821 FDA UDI
FDA Product Code
NXC FDA UDI
GMDN Term
Orthodontic progressive aligner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5470 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic progressive aligner

Clearguide Express by Allesee Aoa-Pro — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic progressive aligner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allesee Aoa-Pro

Sources (1)

  • FDA UDI be82e3d7-cd86-47dd-a527-c1a1f7c20c41 35 fields · synced May 30, 2026