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Silovance

FDA UDI

Class U (US FDA UDI)

by Med Way Inc.

Identity

Trade Name
Silovance FDA UDI
Generic Name
Wound hydrogel dressing, antimicrobial FDA UDI
Device Name
Silovance Curavance Nano SIlver Gel Antibacterial Wound Dressing Gel, 1 Oz. FDA UDI
Model / Reference
1 Oz. FDA UDI
Description
Silovance Curavance Nano SIlver Gel Antibacterial Wound Dressing Gel, 1 Oz. FDA UDI

Identifiers

Primary DI / UDI-DI
00810042271555 FDA UDI
510(k) Number
K092826 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

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 28 Gram FDA UDI

Category: Wound hydrogel dressing, antimicrobial

Silovance by Med Way Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Med Way Inc.

Sources (1)

  • FDA UDI e20159ee-623c-4d62-a71d-2efe56eec0d2 36 fields · synced Jun 8, 2026