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ScarMD

FDA UDI

Class I (US FDA UDI)

by Aim Medical Inc

Identity

Trade Name
ScarMD FDA UDI
Generic Name
Scar management dressing, single-use, sterile FDA UDI
Device Name
ScarMD Silicone Scar Gel 6g Glide FDA UDI
Model / Reference
30mL Spray FDA UDI
Description
ScarMD Silicone Scar Gel 6g Glide FDA UDI

Identifiers

Primary DI / UDI-DI
00860004589747 FDA UDI
FDA Product Code
MDA FDA UDI
GMDN Term
Scar management dressing, single-use, sterile 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Scar management dressing, single-use, sterile

ScarMD by Aim Medical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scar management dressing, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aim Medical Inc

Sources (1)

  • FDA UDI 1bf792b4-3889-4739-80e2-683be7ed9d39 33 fields · synced May 30, 2026