XTRAC

GUDID 010822602

Strata Skin Sciences, Inc.

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• Primary Device ID: 010822602
• NIH Device Record Key: 75862d31-7d03-4436-93f0-730b70fa1108
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: XTRAC
• Version Model Number: AL 8000 Ultra Plus
• Company DUNS: 618522536
• Company Name: Strata Skin Sciences, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• 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	010822602 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041943

FDA Product Code

• GEX: Powered Laser Surgical Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-03-10
• Device Publish Date: 2017-02-13

On-Brand Devices [XTRAC]

• 010822603: AL 8000 Ultra Plus 7 Series
• 010822602: AL 8000 Ultra Plus