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Bingo-Pro

FDA UDI

Class U (US FDA UDI)

by Forum Engineering Technologies (96) Ltd.

Identity

Trade Name
Bingo-Pro FDA UDI
Generic Name
Endodontic apex locator FDA UDI
Device Name
Bingo-Pro Apex Locator FDA UDI
Model / Reference
B-31 FDA UDI
Description
Bingo-Pro Apex Locator FDA UDI

Identifiers

Catalog Number
5-B31-000 FDA UDI
Primary DI / UDI-DI
07290114351003 FDA UDI
510(k) Number
K111474 FDA UDI
FDA Product Code
LQY FDA UDI
GMDN Term
Endodontic apex locator FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endodontic apex locator

Bingo-Pro by Forum Engineering Technologies (96) Ltd. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic apex locator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d066a7fb-0c84-4c43-bb8b-90e88444e447 35 fields · synced May 30, 2026