Fittop

GUDID 06933917000853

Shenzhen Fittop Health Technology Co., Ltd.

Blue/red/infrared phototherapy lamp

• Primary Device ID: 06933917000853
• NIH Device Record Key: bc1c1275-2e8d-4414-bdfc-7a248d9fc266
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fittop
• Version Model Number: FCM902
• Company DUNS: 544301417
• Company Name: Shenzhen Fittop Health Technology Co., Ltd.
• 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: true
• Serial Number: false
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	06933917000853 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K251588

FDA Product Code

• OHS: Light Based Over The Counter Wrinkle Reduction

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: 2025-10-03
• Device Publish Date: 2025-09-25

On-Brand Devices [Fittop]

• 06933917000884: FCM908
• 06933917000877: FCM906
• 06933917000860: FCM905
• 06933917000853: FCM902
• 06933917000846: FCM910