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Lingual Retainer

FDA UDI

Class I (US FDA UDI)

by GC Orthodontics America Inc.

Identity

Trade Name
Lingual Retainer FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Device Name
LGT BOND LING RETAIN SZ 35 FDA UDI
Model / Reference
65-0335-0000 FDA UDI
Description
LGT BOND LING RETAIN SZ 35 FDA UDI

Identifiers

Catalog Number
65-0335-0000 FDA UDI
Primary DI / UDI-DI
D78865033500001 FDA UDI
FDA Product Code
DYJ FDA UDI
GMDN Term
Orthodontic retainer 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

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

No

FDA UDI

Category: Orthodontic retainer

Lingual Retainer by GC Orthodontics America Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic retainer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fae294c1-de2d-4834-a0ce-d6cebbafa39b 35 fields · synced Jun 8, 2026