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Falcon

FDA UDI

Class I (US FDA UDI)

by Ortho Technology, Inc.

Identity

Trade Name
Falcon FDA UDI
Generic Name
Orthodontic pliers FDA UDI
Device Name
Arch Bending Pliers FDA UDI
Model / Reference
800-307 FDA UDI
Description
Arch Bending Pliers FDA UDI

Identifiers

Primary DI / UDI-DI
00190730088512 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Orthodontic pliers 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

Yes

FDA UDI

Category: Orthodontic pliers

Falcon by Ortho Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 81b7b2ff-622d-4841-ae96-0570073763a7 33 fields · synced May 30, 2026