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SUPER VIEW® Disposable Lens Set for ZEISS RESIGHT®

FDA UDI

Class II (US FDA UDI)

by Insight Instruments, Inc.

Identity

Trade Name
SUPER VIEW® Disposable Lens Set for ZEISS RESIGHT® FDA UDI
Generic Name
Ophthalmic diagnostic condensing lens FDA UDI
Device Name
1 Each 40414 RESIGHT® Wide Field Lens and 1 Each 40417 Hassan-Tornambe Contact Lens. Distributed by THEA Surgical (Insight's REF 40226) FDA UDI
Model / Reference
TS-ZR-LS FDA UDI
Description
1 Each 40414 RESIGHT® Wide Field Lens and 1 Each 40417 Hassan-Tornambe Contact Lens. Distributed by THEA Surgical (Insight's REF 40226) FDA UDI

Identifiers

Catalog Number
40226 FDA UDI
Primary DI / UDI-DI
00856222004063 FDA UDI
510(k) Number
K051630 FDA UDI
FDA Product Code
HJK FDA UDI
GMDN Term
Ophthalmic diagnostic condensing lens 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

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

SUPER VIEW® Disposable Lens Set for ZEISS RESIGHT® by Insight Instruments, 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

Sources (1)

  • FDA UDI 6e78b8d5-b206-443d-b36c-f3a7c245095b 37 fields · synced May 30, 2026