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SUPER VIEW® Disposable Lens Set, Pivot Plus

FDA UDI

Class II (US FDA UDI)

by Oculus Surgical Inc

Identity

Trade Name
SUPER VIEW® Disposable Lens Set, Pivot Plus FDA UDI
Generic Name
Vitrectomy contact lens, single-use FDA UDI
Device Name
1 Each SUPER VIEW® Sterile Disposable Pivot Plus Lens Set for use with the SUPER VIEW® System or BIOM® FDA UDI
Model / Reference
40227 FDA UDI
Description
1 Each SUPER VIEW® Sterile Disposable Pivot Plus Lens Set for use with the SUPER VIEW® System or BIOM® FDA UDI

Identifiers

Catalog Number
40227 FDA UDI
Primary DI / UDI-DI
00856222004179 FDA UDI
510(k) Number
K051630 FDA UDI
FDA Product Code
HJK FDA UDI
GMDN Term
Vitrectomy contact lens, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1385 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 13 Millimeter FDA UDI
Outer Diameter — 18 Millimeter FDA UDI
Outer Diameter — 42 Millimeter FDA UDI

Category: Ophthalmic diagnostic condensing lensVitrectomy contact lens, single-use

SUPER VIEW® Disposable Lens Set, Pivot Plus by Oculus Surgical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitrectomy contact lens, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oculus Surgical Inc

Sources (1)

  • FDA UDI 9e1e8e83-72ab-4ea8-8010-70829dd28d96 38 fields · synced Jun 8, 2026