Advanced Seal Wound Barrier, 1oz spray

GUDID 00858071004256

Topical spray on wound dressing, 1oz

Kericure Inc.

Skin-cover sealant

• Primary Device ID: 00858071004256
• NIH Device Record Key: e88d8cba-c993-4d0c-8c7a-fcafaad6fbdc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Advanced Seal Wound Barrier, 1oz spray
• Version Model Number: 2000310
• Company DUNS: 966638681
• Company Name: Kericure 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: true
• 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: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00858071004256 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131384

FDA Product Code

• KMF: Bandage, Liquid

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: 2025-08-29
• Device Publish Date: 2025-08-21

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