SkinPen

GUDID 10863221000320

Case of 12 SkinPen Precision Treatment Kits

BELLUS MEDICAL, LLC

Cosmetic micro-needling electronic handpiece
Primary Device ID10863221000320
NIH Device Record Key1efd35fc-3468-4ccf-b326-678dd2347089
Commercial Distribution StatusIn Commercial Distribution
Brand NameSkinPen
Version Model Number1
Company DUNS005677967
Company NameBELLUS MEDICAL, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110863221000320 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QAIPowered Microneedle Device

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10863221000320]

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Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-07-07
Device Publish Date2018-04-09

On-Brand Devices [SkinPen]

008632210003611
0086322100035424 count of Treatment Kit singles
00863221000347101
00863221000330SkinPen Box (includes SkinPen Precision hand-piece, charging base, and AC Adapter).
00863221000323Treatment kit which includes a sterile, disposable cartridge tip, a hydrogel 510k exempt medical
00863221000316100
00863221000309014
20863221000327Case of 18 single treatment kits.
10863221000320Case of 12 SkinPen Precision Treatment Kits

Trademark Results [SkinPen]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SKINPEN
SKINPEN
85922262 4532187 Live/Registered
Bellus Medical, LLC
2013-05-03

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