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Posterior Direct Bond Bracket Holder

FDA UDI

Class I (US FDA UDI)

by Ortho Organizers, Inc.

Identity

Trade Name
Posterior Direct Bond Bracket Holder FDA UDI
Generic Name
Orthodontic pliers FDA UDI
Device Name
Posterior Direct Bond Bracket Holder FDA UDI
Model / Reference
200-311 FDA UDI
Description
Posterior Direct Bond Bracket Holder FDA UDI

Identifiers

Primary DI / UDI-DI
00190707102371 FDA UDI
FDA Product Code
ECQ FDA UDI
GMDN Term
Orthodontic pliers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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

Category: Orthodontic pliers

Posterior Direct Bond Bracket Holder by Ortho Organizers, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cdb7e0ba-abf8-43a9-a4ba-79edeeb9a1f8 33 fields · synced Jun 9, 2026