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Elastics

FDA UDI

Class I (US FDA UDI)

by GC Orthodontics America Inc.

Identity

Trade Name
ELASTICS FDA UDI
Generic Name
Orthodontic archwire/bracket ligature FDA UDI
Device Name
ELASTICS HV 6MM 6 OZ Baritone 1/4 (NEON) FDA UDI
Model / Reference
85-0641-1111 FDA UDI
Description
ELASTICS HV 6MM 6 OZ Baritone 1/4 (NEON) FDA UDI

Identifiers

Catalog Number
96-0641-1111 FDA UDI
Primary DI / UDI-DI
E53585064111111 FDA UDI
FDA Product Code
ECI FDA UDI
GMDN Term
Orthodontic archwire/bracket ligature 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic archwire/bracket ligature

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

Similar devices

Also classified as Orthodontic archwire/bracket ligature.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ea039201-aca1-41d2-aa5c-3cdd431bec1f 35 fields · synced Jun 8, 2026