← Back to catalogue

Scar Aid

FDA UDI

Class I (US FDA UDI)

by Biodermis Llc

Identity

Trade Name
SCAR AID FDA UDI
Generic Name
Scar-management dressing, reusable FDA UDI
Device Name
SCAR AID SILICONE STICK 17g FDA UDI
Model / Reference
SCST17-US FDA UDI
Description
SCAR AID SILICONE STICK 17g FDA UDI

Identifiers

Catalog Number
SCST17-US FDA UDI
Primary DI / UDI-DI
00850014883188 FDA UDI
510(k) Number
K992146 FDA UDI
FDA Product Code
MDA FDA UDI
GMDN Term
Scar-management dressing, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4025 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

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
MRI Safety
MR Conditional FDA UDI

Category: Scar-management dressing, reusable

Scar Aid by Biodermis Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scar-management dressing, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biodermis Llc

Sources (1)

  • FDA UDI ba9ad4cf-5fb5-44a6-a759-028393e5f9c1 36 fields · synced Jun 8, 2026