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Ortho Arch

FDA UDI

Class I (US FDA UDI)

by Ortho Arch Company Inc

Identity

Trade Name
ORTHO ARCH FDA UDI
Generic Name
Orthodontic archwire/bracket ligature FDA UDI
Device Name
.010 KOBAYASHI HOOKS (100) **WHILE SUPPLIES LAST. DISCONTINUED ITEM. NON-REFUNDABLE** FDA UDI
Model / Reference
.010 KOBAYASHI HOOKS FDA UDI
Description
.010 KOBAYASHI HOOKS (100) **WHILE SUPPLIES LAST. DISCONTINUED ITEM. NON-REFUNDABLE** FDA UDI

Identifiers

Catalog Number
270-001 FDA UDI
Primary DI / UDI-DI
D9092700011 FDA UDI
FDA Product Code
DZD 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic archwire/bracket ligature

Ortho Arch by Ortho Arch Company 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 ef4ee31c-222b-4a43-b0f4-e435cd2d0a27 34 fields · synced Jun 1, 2026