Q-SWITCHED ND:YAG LASER

GUDID 06975617992014

BEIJING HONKON TECHNOLOGIES CO., LTD.

Dermatological frequency-doubled solid-state laser system

• Primary Device ID: 06975617992014
• NIH Device Record Key: c1c56a0f-6033-4ec3-9142-ec83af235ecd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Q-SWITCHED ND:YAG LASER
• Version Model Number: 1064
• Company DUNS: 529481958
• Company Name: BEIJING HONKON TECHNOLOGIES CO., LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975617992014 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2026-03-31
• Device Publish Date: 2026-03-23

Devices Manufactured by BEIJING HONKON TECHNOLOGIES CO., LTD.

• 06975617991024 - DIODE LASER FOR HIAR REMOVAL: 2026-03-31
• 06975617992014 - Q-SWITCHED ND:YAG LASER: 2026-03-31
• 06975617992014 - Q-SWITCHED ND:YAG LASER: 2026-03-31
• 06975617993011 - CO2 FRACTIONAL LASER: 2026-03-31
• 06975617994025 - MULTIFUNCTIONAL SERIES: 2026-03-31
• 06975617995039 - SLIMMING TREATMENT DEVICE: 2026-03-31