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Twin Force® Bite Corrector

FDA UDI

Class I (US FDA UDI)

by Ortho Organizers, Inc.

Identity

Trade Name
Twin Force® Bite Corrector FDA UDI
Generic Name
Orthodontic habit prevention/breaking appliance, bonded FDA UDI
Device Name
Twin Force® Bite Corrector Anchor Wire (Small, 27-36mm) FDA UDI
Model / Reference
424-211TI FDA UDI
Description
Twin Force® Bite Corrector Anchor Wire (Small, 27-36mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00190707059255 FDA UDI
FDA Product Code
EJF FDA UDI
GMDN Term
Orthodontic habit prevention/breaking appliance, bonded 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

Yes

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

Category: Orthodontic habit prevention/breaking appliance, bonded

Twin Force® Bite Corrector by Ortho Organizers, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic habit prevention/breaking appliance, bonded.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ef5d3503-c99f-4e5a-b3a2-6d1fcb0bf7c3 33 fields · synced Jun 9, 2026