Nasal Implant 402-101

GUDID B490402101

Nasal Style 1 Size 1

Aart

Nasal cartilage support implant, non-bioabsorbable

• Primary Device ID: B490402101
• NIH Device Record Key: b07cf045-da23-467d-808c-a47f338d4dcd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nasal Implant
• Version Model Number: D
• Catalog Number: 402-101
• Company DUNS: 091356894
• Company Name: Aart
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com
• Phone: (775) 853-6800
• Email: customer.service@alphaaesthetics.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B490402101 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K021418

FDA Product Code

• FZE: Prosthesis, Nose, Internal

Sterilization

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

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

[B490402101]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-05
• Device Publish Date: 2025-08-28

On-Brand Devices [Nasal Implant]

• B490402505: Nasal Style 5 Size 5
• B490402404: Nasal Style 4 Size 4
• B490402303: Nasal Style 3 Size 3
• B490402202: Nasal Style 2 Size 2
• B490402101: Nasal Style 1 Size 1