ArtMost SoftOK Daily Wear Soft Contact Lens

FDA UDI

Class II (US FDA UDI)

by Seinoh Optical Co., Ltd.

Identity

Trade Name: ArtMost SoftOK Daily Wear Soft Contact Lens FDA UDI
Generic Name: Soft corrective contact lens, daily-wear FDA UDI
Device Name: 6 sterile daily wear soft contact lenses, 45% Ocufilcon D, 55% water. FDA UDI
Model / Reference: STC/-5.75D FDA UDI
Description: 6 sterile daily wear soft contact lenses, 45% Ocufilcon D, 55% water. FDA UDI

Identifiers

Primary DI / UDI-DI: 04719891034730 FDA UDI
510(k) Number: K141280 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

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 14.4 Millimeter FDA UDI

Category: Soft corrective contact lens, daily-wear

ArtMost SoftOK Daily Wear Soft Contact Lens by Seinoh Optical Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K141280 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Seinoh Optical Co., Ltd.

Sources (1)

FDA UDI a2ff2cf4-fe73-4091-94cb-fa2f9593821a 36 fields · synced Jun 1, 2026