ScarMD

GUDID 00383160000067

ScarMD Silicone Scar Gel

AIM MEDICAL INC.

Scar-management dressing, single-use
Primary Device ID00383160000067
NIH Device Record Key580ef696-d2ed-4699-840e-a62d6cbf0b50
Commercial Distribution StatusIn Commercial Distribution
Brand NameScarMD
Version Model Number3g CN
Company DUNS117589740
Company NameAIM MEDICAL INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100383160000067 [Primary]

FDA Product Code

MDAElastomer, Silicone, For Scar Management

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-23
Device Publish Date2024-07-15

On-Brand Devices [ScarMD]

00860004589709ScarMD Silicone Scar Gel, 15g
00860004589747ScarMD Silicone Scar Spray 30mL
00860004589730ScarMD Silicone Scar Gel 3g
00860004589723ScarMD Silicone Scar Gel 6g
00860004589716ScarMD silicone scar gel 15g Glide Massaging
00860004589778ScarMD Silicone Scar Gel 1g
00383160000005ScarMD Silicone Scar Gel
00860004589785ScarMD Silicone Scar Gel 6g Glide
00383160000081ScarMD Silicone Scar Gel 6g Glide
00383160000074ScarMD Silicone Scar Gel 1g
00383160000067ScarMD Silicone Scar Gel
00383160000050ScarMD Silicone Scar Gel
00383160000043ScarMD Silicone Scar Gel 15g Glide
00383160000036ScarMD Silicone Scar Gel 15g

Trademark Results [ScarMD]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SCARMD
SCARMD
90772287 not registered Live/Pending
AIM MEDICAL INC.
2021-06-14

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.