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Clearviz Mini

FDA UDI

Class II (US FDA UDI)

by Ortho Solutions LC

Identity

Trade Name
CLEARVIZ MINI FDA UDI
Generic Name
Orthodontic bracket, ceramic FDA UDI
Device Name
ORTHODONTIC CERAMIC/PLASTIC BRACKET FDA UDI
Model / Reference
300XX FDA UDI
Description
ORTHODONTIC CERAMIC/PLASTIC BRACKET FDA UDI

Identifiers

Primary DI / UDI-DI
D841300XX18 FDA UDI
FDA Product Code
NJM FDA UDI
GMDN Term
Orthodontic bracket, ceramic 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic bracket, ceramic

Clearviz Mini by Ortho Solutions LC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic bracket, ceramic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ortho Solutions LC

Sources (1)

  • FDA UDI 4def67e1-631b-4997-890c-42caaf4f5a41 33 fields · synced Jun 8, 2026