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InkWell Health

FDA UDI

Class I (US FDA UDI)

by Inkwell Health

Identity

Trade Name
InkWell Health FDA UDI
Generic Name
Skin marking guide, single-use FDA UDI
Device Name
InkWell Health Large Right Knee Temporary Tattoo FDA UDI
Model / Reference
LGRKNEE-MTT FDA UDI
Description
InkWell Health Large Right Knee Temporary Tattoo FDA UDI

Identifiers

Primary DI / UDI-DI
00860010334522 FDA UDI
FDA Product Code
FZZ FDA UDI
GMDN Term
Skin marking guide, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4660 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

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: Skin marking guide, single-use

InkWell Health by Inkwell Health — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin marking guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inkwell Health

Sources (1)

  • FDA UDI de8ea61a-9fe2-4ce2-9551-4677af9cfacb 33 fields · synced May 30, 2026