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Solo-Pack

FDA UDI

Class I (US FDA UDI)

by G&H Wire Company, Inc.

Identity

Trade Name
SOLO-PACK FDA UDI
Generic Name
Orthodontic archwire FDA UDI
Device Name
Stainless Steel, .018x.025 (,46mm x ,64mm), Lower, Bioform III, Aesthetic, Solo-Pack FDA UDI
Model / Reference
SSBF3L1825AES FDA UDI
Description
Stainless Steel, .018x.025 (,46mm x ,64mm), Lower, Bioform III, Aesthetic, Solo-Pack FDA UDI

Identifiers

Primary DI / UDI-DI
10190886232903 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
Width — .025 Inch FDA UDI
Height — .018 Inch FDA UDI

Category: Orthodontic archwire

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 3c1ae424-7696-43ab-b3a5-3145dedec957 35 fields · synced Jun 8, 2026