← Back to catalogue

LP Low Profile

FDA UDI

Class I (US FDA UDI)

by American Orthodontics

Identity

Trade Name
LP Low Profile FDA UDI
Generic Name
Orthodontic tube FDA UDI
Device Name
TUBE FLANGELESS LP MAND RIGHT 2ND MOLAR 018 CAST NON-CONV T-25 A=0 R=5 3.2MM FDA UDI
Model / Reference
004-3012CF FDA UDI
Description
TUBE FLANGELESS LP MAND RIGHT 2ND MOLAR 018 CAST NON-CONV T-25 A=0 R=5 3.2MM FDA UDI

Identifiers

Catalog Number
004-3012CF FDA UDI
Primary DI / UDI-DI
00190746138225 FDA UDI
FDA Product Code
DZD FDA UDI
GMDN Term
Orthodontic tube FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

LP Low Profile by American Orthodontics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f91f937d-8cf6-433f-95aa-f7eeee6419de 36 fields · synced Jun 9, 2026