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A2

FDA UDI

Class I (US FDA UDI)

by Reliance Orthodontic Products, Inc.

Identity

Trade Name
A2 FDA UDI
Generic Name
Dental mould FDA UDI
Device Name
A2 Oval Attachment Form can be used for the retention of themoplastic aligners and for horizontal or vertical placement on the tooth depending on the height of the crown. FDA UDI
Model / Reference
AO FDA UDI
Description
A2 Oval Attachment Form can be used for the retention of themoplastic aligners and for horizontal or vertical placement on the tooth depending on the height of the crown. FDA UDI

Identifiers

Catalog Number
AO FDA UDI
Primary DI / UDI-DI
D798AO1 FDA UDI
FDA Product Code
KXR FDA UDI
GMDN Term
Dental mould FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3140 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

A2 by Reliance Orthodontic Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2c97e97c-c75b-488b-b381-9c4e9d6d1c50 37 fields · synced Jun 8, 2026