← Back to catalogue

Intraoral Cheek Retractors

FDA UDI

Class I (US FDA UDI)

by Ortho Technology, Inc.

Identity

Trade Name
Intraoral Cheek Retractors FDA UDI
Generic Name
Dental cheek retractor, professional, single-use FDA UDI
Device Name
Retractor Intraoral Lg 10/pk FDA UDI
Model / Reference
601-222 FDA UDI
Description
Retractor Intraoral Lg 10/pk FDA UDI

Identifiers

Primary DI / UDI-DI
00190730032966 FDA UDI
FDA Product Code
EIF FDA UDI
GMDN Term
Dental cheek retractor, professional, single-use 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

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

Yes

FDA UDI

Category: Dental cheek retractor, professional, single-use

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

Similar devices

Also classified as Dental cheek retractor, professional, single-use.

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 f88c9d5f-de0b-4bcf-a6d2-d3feef4991b4 33 fields · synced May 30, 2026