← Back to catalogue

Ortho Arch

FDA UDI

Class I (US FDA UDI)

by Ortho Arch Company Inc

Identity

Trade Name
ORTHO ARCH FDA UDI
Generic Name
Orthodontic appliance dimension gauge FDA UDI
Device Name
BOLEY GAUGE CURVED ***DISCONTINUED/ WHILE SUPPLIES LAST. NON-REFUNDABLE OR RETURNABLE*** FDA UDI
Model / Reference
800-081C FDA UDI
Description
BOLEY GAUGE CURVED ***DISCONTINUED/ WHILE SUPPLIES LAST. NON-REFUNDABLE OR RETURNABLE*** FDA UDI

Identifiers

Primary DI / UDI-DI
D909800081C1 FDA UDI
FDA Product Code
EIL FDA UDI
GMDN Term
Orthodontic appliance dimension gauge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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 appliance dimension gauge

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 appliance dimension gauge.

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

Sources (1)

  • FDA UDI 902db794-2fb8-4e9e-bf92-5d15e2dfd661 33 fields · synced May 30, 2026