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DMV MiniCup

FDA UDI

Class I (US FDA UDI)

by DMV Corporation

Identity

Trade Name
DMV MiniCup FDA UDI
Generic Name
Rigid contact lens inserter/remover FDA UDI
Device Name
Contact lens remover/inserter with a smaller and deeper cup for small hard and gp contact lenses. FDA UDI
Model / Reference
529 FDA UDI
Description
Contact lens remover/inserter with a smaller and deeper cup for small hard and gp contact lenses. FDA UDI

Identifiers

Catalog Number
529 FDA UDI
Primary DI / UDI-DI
00080875975290 FDA UDI
510(k) Number
K830496 FDA UDI
FDA Product Code
KYE FDA UDI
GMDN Term
Rigid contact lens inserter/remover FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rigid contact lens inserter/remover

DMV MiniCup by DMV Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid contact lens inserter/remover.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DMV Corporation

Sources (1)

  • FDA UDI 5c4c3bc4-d474-425a-b296-47d4402111f8 35 fields · synced May 30, 2026