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Intrigue

FDA UDI

Class II (US FDA UDI)

by Lancer Orthodontics, Inc.

Identity

Trade Name
Intrigue FDA UDI
Generic Name
Orthodontic bracket, metal FDA UDI
Device Name
INTRG WHISP ROTH 2BIC HK-22T 0A 018 LR FDA UDI
Model / Reference
231-071 FDA UDI
Description
INTRG WHISP ROTH 2BIC HK-22T 0A 018 LR FDA UDI

Identifiers

Primary DI / UDI-DI
00817573021062 FDA UDI
FDA Product Code
NJM FDA UDI
GMDN Term
Orthodontic bracket, metal FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5470 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 bracket, metal

Intrigue by Lancer Orthodontics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic bracket, metal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 35a0e054-56a1-46ae-ad20-9fe18990792c 33 fields · synced May 31, 2026