← Back to catalogue

Light Bond

FDA UDI

Class II (US FDA UDI)

by Reliance Orthodontic Products, Inc.

Identity

Trade Name
Light Bond FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
L.C.R™is a flowable, light cure orthodontic adhesive intended to be used within an orthodontic, dental or pediatric dental office for the bonding of lingual retainers, creation of occlusal buildups and for retention of thermoplastic aligners. This kit contains 4 X 5g LCR Adhesive paste in push syringes, 2 X 3cc Light Bond Sealant, 1 X 23g Etchant and mixing accessories. FDA UDI
Model / Reference
LCREP FDA UDI
Description
L.C.R™is a flowable, light cure orthodontic adhesive intended to be used within an orthodontic, dental or pediatric dental office for the bonding of lingual retainers, creation of occlusal buildups and for retention of thermoplastic aligners. This kit contains 4 X 5g LCR Adhesive paste in push syringes, 2 X 3cc Light Bond Sealant, 1 X 23g Etchant and mixing accessories. FDA UDI

Identifiers

Catalog Number
LCREP FDA UDI
Primary DI / UDI-DI
D798LCREP0 FDA UDI
510(k) Number
K894564 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 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

Yes

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

Category: Dental composite resin

Light Bond by Reliance Orthodontic Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

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 701e196a-549f-4a72-8657-6a4348f5dca5 37 fields · synced Jun 1, 2026