Arnett Lefort Implant ALI-M

GUDID M724ALIM1

Malar Implant

IMPLANTECH ASSOCIATES, INC.

Malar prosthesis

• Primary Device ID: M724ALIM1
• NIH Device Record Key: dede7f3a-2801-499e-9632-7ffce1407856
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arnett Lefort Implant
• Version Model Number: Size: Medium
• Catalog Number: ALI-M
• Company DUNS: 784664955
• Company Name: IMPLANTECH ASSOCIATES, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-733-0833
• Email: info@implantech.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M724ALIM1 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K942420

FDA Product Code

• LZK: Implant, Malar

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-14
• Device Publish Date: 2015-09-24

On-Brand Devices [Arnett Lefort Implant]

• M724ALIS1: Malar Implant
• M724ALIM1: Malar Implant
• M724ALIL1: Malar Implant