Advanced Seal Wound Barrier, 1oz spray

FDA UDI

Class I (US FDA UDI)

by Kericure Inc.

Identity

Trade Name: Advanced Seal Wound Barrier, 1oz spray FDA UDI
Generic Name: Skin-cover sealant FDA UDI
Device Name: Topical spray on wound dressing, 1oz FDA UDI
Model / Reference: 2000310 FDA UDI
Description: Topical spray on wound dressing, 1oz FDA UDI

Identifiers

Primary DI / UDI-DI: 00858071004256 FDA UDI
510(k) Number: K131384 FDA UDI
FDA Product Code: KMF FDA UDI
GMDN Term: Skin-cover sealant FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5090 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Skin-cover sealant

Advanced Seal Wound Barrier, 1oz spray by Kericure Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Kericure Inc.

Sources (1)

FDA UDI e88d8cba-c993-4d0c-8c7a-fcafaad6fbdc 34 fields · synced May 30, 2026