AYON Base Tower

GUDID 00607151050498

APYX MEDICAL CORPORATION

Liposuction system

• Primary Device ID: 00607151050498
• NIH Device Record Key: 9f37bdc2-e202-4347-b874-bf74d4955b60
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AYON Base Tower
• Version Model Number: AYON-TOWER
• Company DUNS: 101223287
• Company Name: APYX MEDICAL CORPORATION
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607151050498 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K244050

FDA Product Code

• QPB: System, Suction, Lipoplasty For Removal

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-06
• Device Publish Date: 2025-05-29

On-Brand Devices [AYON Base Tower]

• 00607151050511: AYON-TOWER
• 00607151050498: AYON-TOWER