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BEYOND® II Cheek Retractor (5 pack)

FDA UDI

Class I (US FDA UDI)

by Beyond International Inc.

Identity

Trade Name
BEYOND® II Cheek Retractor (5 pack) FDA UDI
Generic Name
Dental cheek retractor, professional, single-use FDA UDI
Model / Reference
BY-M012 FDA UDI

Identifiers

Primary DI / UDI-DI
00857848007292 FDA UDI
FDA Product Code
EIG 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

BEYOND® II Cheek Retractor (5 pack) by Beyond International 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

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Manufacturer

Sources (1)

  • FDA UDI 4421e8c0-57b0-4812-a49d-4bc060f70d7d 32 fields · synced Jun 9, 2026