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Enlight LV

FDA UDI

Class II (US FDA UDI)

by Ormco Corporation

Identity

Trade Name
Enlight LV FDA UDI
Generic Name
Orthodontic bracket adhesive FDA UDI
Device Name
Low Viscosity Light Cure Adhesive - Unidose Refill FDA UDI
Model / Reference
740-0278 FDA UDI
Description
Low Viscosity Light Cure Adhesive - Unidose Refill FDA UDI

Identifiers

Primary DI / UDI-DI
00889989080179 FDA UDI
FDA Product Code
DYH FDA UDI
GMDN Term
Orthodontic bracket adhesive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3750 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 4 Gram FDA UDI

Category: Orthodontic bracket adhesive

Enlight LV by Ormco Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic bracket adhesive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ormco Corporation

Sources (1)

  • FDA UDI 62513bf7-1a2b-4084-b78e-9fc21a6d887f 36 fields · synced Jun 9, 2026