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ClassOne

FDA UDI

Class II (US FDA UDI)

by Ortho Organizers, Inc.

Identity

Trade Name
ClassOne FDA UDI
Generic Name
Orthodontic extraoral headgear FDA UDI
Device Name
FACEMASK- TURQUOISE FDA UDI
Model / Reference
874-0323 FDA UDI
Description
FACEMASK- TURQUOISE FDA UDI

Identifiers

Primary DI / UDI-DI
00190707004842 FDA UDI
510(k) Number
K000358 FDA UDI
FDA Product Code
DZB FDA UDI
GMDN Term
Orthodontic extraoral headgear FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5500 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic extraoral headgear

ClassOne by Ortho Organizers, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic extraoral headgear.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b9ffa185-88ea-479a-bdfd-d5fb9d187504 34 fields · synced Jun 9, 2026