Pendex

Basic Information

• Brand Name: Pendex
• Primary DI: 00889989087994
• Version / Model: 3000-0092
• Company Name: ALLESEE AOA-PRO
• Labeler DUNS: 158312728
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2023-04-05
• Public Version: 1
• Public Version Date: 2023-04-13
• Public Version Status: New
• Public Device Record Key: 0b6a6bfe-a984-41c1-8b41-676ffa0d35f7

Device Description

Pendex

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
KMY	POSITIONER, TOOTH, PREFORMED	Dental	872.5525	1

GMDN Terms

Code	Name	Definition	Implantable	Status
65678	Orthodontic palate expander screw, self-removable	An orthodontic device intended to be used as part of a self-removable palate expander to gradually spread the maxillary arch to create space for teeth alignment. It is in the form of a threaded rod with expandable pins of various lengths; it is not fixed to the oral cavity so that it can be temporarily removed by the patient during the treatment period (e.g., for eating). This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00889989087994	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]