← Back to catalogue

SmartArch

FDA UDI

Class I (US FDA UDI)

by Smarter Alloys Inc

Identity

Trade Name
SmartArch FDA UDI
Generic Name
Orthodontic archwire FDA UDI
Device Name
SmartArch .018 x .025" (0.457 x 0.635mm) Round Damon Lower Orthodontic CuNiTi Archwire FDA UDI
Model / Reference
SAO-DREL-1825 FDA UDI
Description
SmartArch .018 x .025" (0.457 x 0.635mm) Round Damon Lower Orthodontic CuNiTi Archwire FDA UDI

Identifiers

Primary DI / UDI-DI
D948SAODREL18250 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic archwire

SmartArch by Smarter Alloys 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Smarter Alloys Inc

Sources (1)

  • FDA UDI fa7e07dc-a65a-448b-860e-5864d6283298 33 fields · synced May 29, 2026