AUVON

GUDID 16973810850398

Shenzhen Jian Feng Electronic Technology Co., Ltd.

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 16973810850398
• NIH Device Record Key: a9074410-5fdb-42ac-9d6f-02c5805fc00a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AUVON
• Version Model Number: TA2224C
• Company DUNS: 560082555
• Company Name: Shenzhen Jian Feng Electronic Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com
• Phone: +1(678)829-7256
• Email: support@iauvon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	06973810850391 [Primary]
GS1	16973810850398 [Package]; Contains: 06973810850391; Package: [60 Units]; In Commercial Distribution
GS1	26973810850395 [Package]; Contains: 06973810850391; Package: [48 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223825

FDA Product Code

• NGX: Stimulator, Muscle, Powered, For Muscle Conditioning

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: 2024-11-11
• Device Publish Date: 2024-11-01

Devices Manufactured by Shenzhen Jian Feng Electronic Technology Co., Ltd.

• 16973810850411 - No: 2025-03-19
• 16973810850381 - AVCOO: 2025-01-06
• 16973810850404 - AVCOO: 2024-12-23
• 16973810850398 - AUVON: 2024-11-11
• 16973810850398 - AUVON: 2024-11-11
• 16973810850374 - No: 2024-09-12
• 16973810850350 - No: 2024-08-29
• 16973810850367 - No: 2024-08-29
• 16973810850343 - No: 2024-08-21