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DMV Vented Scleral Cup

FDA UDI

Class I (US FDA UDI)

by DMV Corporation

Identity

Trade Name
DMV Vented Scleral Cup FDA UDI
Generic Name
Rigid contact lens inserter/remover FDA UDI
Device Name
Contact lens Inserter with air channel for inserting hybrid, large soft and gp contact lenses. No suction FDA UDI
Model / Reference
110 FDA UDI
Description
Contact lens Inserter with air channel for inserting hybrid, large soft and gp contact lenses. No suction FDA UDI

Identifiers

Catalog Number
110 FDA UDI
Primary DI / UDI-DI
00080875971100 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 Vented Scleral Cup 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 c16f01fd-0b06-48b8-82d8-653b72392b34 35 fields · synced Jun 1, 2026