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Another Me Kristin Monthly

FDA UDI

Class II (US FDA UDI)

by DK MEDIVISION Co., Ltd.

Identity

Trade Name
Another Me Kristin Monthly FDA UDI
Generic Name
Soft corrective contact lens, daily-wear FDA UDI
Device Name
Another Me Kristin Monthly/Hazel Color/0.00/50EA FDA UDI
Model / Reference
Another Me Kristin Monthly FDA UDI
Description
Another Me Kristin Monthly/Hazel Color/0.00/50EA FDA UDI

Identifiers

Primary DI / UDI-DI
08800071415107 FDA UDI
510(k) Number
K220045 FDA UDI
FDA Product Code
LPL FDA UDI
GMDN Term
Soft corrective contact lens, daily-wear FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.5925 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Soft corrective contact lens, daily-wear

Another Me Kristin Monthly by DK MEDIVISION Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft corrective contact lens, daily-wear.

Cleared under the same submission

K220045 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DK MEDIVISION Co., Ltd.

Sources (1)

  • FDA UDI 36d98996-a786-4dea-a9c9-4ec76daf8ad4 34 fields · synced Jun 1, 2026