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revyve Antimicrobial Wound Gel Spray

FDA UDI

Class U (US FDA UDI)

by Kane Biotech, Inc.

Identity

Trade Name
revyve Antimicrobial Wound Gel Spray FDA UDI
Generic Name
Wound hydrogel dressing, antimicrobial FDA UDI
Device Name
revyve™ Antimicrobial Wound Gel is a clear, odorless gel that provides a moist wound environment conducive to healing. revyve™ Antimicrobial Wound Gel provides preservative properties through an antimicrobial (PHMB) to help inhibit microbial colonization within the gel during shelf storage. Chronic wounds are known to contain non-viable tissue. revyve™ Antimicrobial Wound Gel can facilitate debridement through a moist wound environment. FDA UDI
Model / Reference
CWG142S FDA UDI
Description
revyve™ Antimicrobial Wound Gel is a clear, odorless gel that provides a moist wound environment conducive to healing. revyve™ Antimicrobial Wound Gel provides preservative properties through an antimicrobial (PHMB) to help inhibit microbial colonization within the gel during shelf storage. Chronic wounds are known to contain non-viable tissue. revyve™ Antimicrobial Wound Gel can facilitate debridement through a moist wound environment. FDA UDI

Identifiers

Primary DI / UDI-DI
00628451217725 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound hydrogel dressing, antimicrobial FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound hydrogel dressing, antimicrobial

revyve Antimicrobial Wound Gel Spray by Kane Biotech, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kane Biotech, Inc.

Sources (1)

  • FDA UDI 29de2567-4361-4fac-90de-dc67880e97e3 33 fields · synced May 30, 2026