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ApexPilot

FDA UDI

Class U (US FDA UDI)

by Beyes Dental Canada Inc

Identity

Trade Name
ApexPilot FDA UDI
Generic Name
Endodontic apex locator FDA UDI
Device Name
ApexPilot , Apex Locator, Rechargeable Battery FDA UDI
Model / Reference
AL2040 FDA UDI
Description
ApexPilot , Apex Locator, Rechargeable Battery FDA UDI

Identifiers

Catalog Number
ApexPilot FDA UDI
Primary DI / UDI-DI
00990010301351 FDA UDI
510(k) Number
K181087 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Endodontic apex locator

ApexPilot by Beyes Dental Canada Inc — 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 43c71c92-8f0e-4c00-814b-5157b4ae3fc8 35 fields · synced Jun 8, 2026