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Rectangular RCS Nickel Titanium Archwire

FDA UDI

Class I (US FDA UDI)

by Ortho Arch Company Inc

Identity

Trade Name
Rectangular RCS Nickel Titanium Archwire FDA UDI
Generic Name
Orthodontic archwire FDA UDI
Device Name
.016 X .016 NITINOL Rectangular RCS Style E with Dimple UPPER FDA UDI
Model / Reference
226-370 FDA UDI
Description
.016 X .016 NITINOL Rectangular RCS Style E with Dimple UPPER FDA UDI

Identifiers

Catalog Number
226-370 FDA UDI
Primary DI / UDI-DI
D90922637017 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

No

FDA UDI

Category: Orthodontic archwire

Rectangular RCS Nickel Titanium Archwire by Ortho Arch 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 1956c5f3-d7fc-4a17-b6df-7ffb63e9f608 34 fields · synced May 31, 2026