PMD

GUDID 00811485037210

Shenzhen Fittop Health Technology Co., Ltd.

Blue/red/infrared phototherapy lamp

• Primary Device ID: 00811485037210
• NIH Device Record Key: 6e7f1808-57b0-435c-98c6-d8f9daadd997
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PMD
• Version Model Number: 11-001-RBMASK
• 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	00811485037210 [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: 2026-01-26
• Device Publish Date: 2026-01-16

Devices Manufactured by Shenzhen Fittop Health Technology Co., Ltd.

• 00811485037210 - PMD: 2026-01-26
• 00811485037210 - PMD: 2026-01-26
• 06933917000846 - Fittop: 2025-10-03
• 06933917000853 - Fittop: 2025-10-03
• 06933917000860 - Fittop: 2025-10-03
• 06933917000877 - Fittop: 2025-10-03
• 06933917000884 - Fittop: 2025-10-03