TheraClear 20TC129

GUDID B30520TC1290

THERAVANT CORPORATION

Multi-modality skin surface treatment system generator

• Primary Device ID: B30520TC1290
• NIH Device Record Key: 140fab61-bab7-49c8-9d6f-6c44ef3ffdc7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TheraClear
• Version Model Number: 20TC12900AA
• Catalog Number: 20TC129
• Company DUNS: 927989959
• Company Name: THERAVANT CORPORATION
• 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: true
• Lot Batch: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B30520TC1290 [Primary]
HIBCC	B30520TC1291 [Package]; Package: Box [20 Units]; In Commercial Distribution
HIBCC	B30520TC1292 [Package]; Package: Box [10 Units]; In Commercial Distribution

FDA Product Code

• ONF: Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-20

On-Brand Devices [TheraClear]

• B305THERACLEAR10: 40-TC116-00.AA
• B30530TC0730: 30TC073AA00
• B30530TC0300: 30TC03000AA
• B30520TC1290: 20TC12900AA