AccessGUDID - DEVICE: Propex-Pixi Apex Locator (D100A103000000200)

GUDID

Device Identifier (DI) Information

Brand Name: Propex-Pixi Apex Locator
Version or Model: 1
Commercial Distribution Status: In Commercial Distribution
Catalog Number: A103000000200
Company Name: FORUM ENGINEERING TECHNOLOGIES (96) LTD.

Primary DI Number: D100A103000000200
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 532219235 *Terms of Use

Device Description: Propex-Pixi Apex Locator

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
16355	Endodontic apex locator	A dental instrument, using electricity, designed to locate the top of the root canal during endodontic procedures. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LQY	Locator, Root Apex

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K121206	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f5a617f6-e8bd-47be-8e12-6ca8194b1a3e
Public Version Date: February 02, 2026
Public Version Number: 1
DI Record Publish Date: January 23, 2026