FDA UDI In Commercial Distribution 🇺🇸 United States

NanoPen

DI: 00850061586018 · Model: Pro · Zizion Group Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NanoPen
Primary DI
00850061586018
Version / Model
Pro
Company Name
Zizion Group Inc.
Labeler DUNS
013220824
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-26
Public Version
1
Public Version Date
2025-01-03
Public Version Status
New
Public Device Record Key
0535f93e-2332-482f-8c64-3c508eeb8aaa

Device Description

NanoPen Pro Assembly ( Includes NanoPen Pro hand-piece and AC Adapter

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QAI Powered Microneedle Device

GMDN Terms

Code Name
61216 Cosmetic micro-needling electronic handpiece, professional

Identifiers

Type ID
Primary 00850061586018

Premarket Submissions

Submission Number Supplement Number
K230420 000