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Cobo 6.5mm Temporary Keratoprothesis

FDA UDI

Class II (US FDA UDI)

by Ocular Instruments, Inc.

Identity

Trade Name
Cobo 6.5mm Temporary Keratoprothesis FDA UDI
Generic Name
Vitrectomy contact lens, reusable FDA UDI
Model / Reference
OCTK-6.5 FDA UDI

Identifiers

Primary DI / UDI-DI
00630238008921 FDA UDI
510(k) Number
K895013 FDA UDI
FDA Product Code
MLP FDA UDI
GMDN Term
Vitrectomy contact lens, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.3400 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

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Vitrectomy contact lens, reusable

Cobo 6.5mm Temporary Keratoprothesis by Ocular Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitrectomy contact lens, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a85b093c-a009-42e4-8c08-b2b350b8bd61 33 fields · synced May 30, 2026