Sublime Applicator, Profound Matrix

GUDID 00817495023755

Candela Corporation

Multi-modality skin surface treatment system

• Primary Device ID: 00817495023755
• NIH Device Record Key: c7b50735-02fe-42fa-b9d2-50b958df3ce5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sublime Applicator, Profound Matrix
• Version Model Number: FG71871
• Company DUNS: 053468385
• Company Name: Candela Corporation
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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
GS1	00817495023755 [Primary]
GS1	07290109952987 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211217

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2022-10-12
• Device Publish Date: 2022-09-16

On-Brand Devices [Sublime Applicator, Profound Matrix]

• 07290109952987: FG71871
• 00817495023755: FG71871