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Ortho Pro

FDA UDI

Class I (US FDA UDI)

by Ortho Pro Dent LLC

Identity

Trade Name
Ortho Pro FDA UDI
Generic Name
Orthodontic wire FDA UDI
Device Name
Bondable Lingual Retainers Mandibular 33 mm 10 pcs/pk FDA UDI
Model / Reference
CSS-LR-B42 FDA UDI
Description
Bondable Lingual Retainers Mandibular 33 mm 10 pcs/pk FDA UDI

Identifiers

Primary DI / UDI-DI
00810152826386 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Orthodontic wire 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic wire

Ortho Pro by Ortho Pro Dent LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic wire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ortho Pro Dent LLC

Sources (1)

  • FDA UDI f9b1b152-4724-4c90-84b1-53a094861f28 35 fields · synced May 30, 2026