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G4 Ultraesthetic Nickel Titanium Solo-Pack

FDA UDI

Class I (US FDA UDI)

by G&H Wire Company, Inc.

Identity

Trade Name
G4 ULTRAESTHETIC NICKEL TITANIUM SOLO-PACK FDA UDI
Generic Name
Orthodontic archwire FDA UDI
Device Name
G4 NITI RCI UPR 020 TOOTH SOLO-PACK FDA UDI
Model / Reference
G4RCU020TS FDA UDI
Description
G4 NITI RCI UPR 020 TOOTH SOLO-PACK FDA UDI

Identifiers

Primary DI / UDI-DI
10190886017395 FDA UDI
FDA Product Code
DZC FDA UDI
GMDN Term
Orthodontic archwire 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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — .020 Inch FDA UDI

Category: Orthodontic archwire

G4 Ultraesthetic Nickel Titanium Solo-Pack by G&H Wire Company, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic archwire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ee1d014e-beea-4eb1-9c73-bd4b31bb8b47 35 fields · synced Jun 8, 2026