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SUPER VIEW® Lens Set, HD Plus, Disposable for ZEISS RESIGHT®
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- SUPER VIEW® Lens Set, HD Plus, Disposable for ZEISS RESIGHT® FDA UDI
- Generic Name
- Ophthalmic diagnostic condensing lens FDA UDI
- Device Name
- 1 Each SUPER VIEW® Sterile Disposable HD Plus Lens Set for use with ZEISS RESIGHT® FDA UDI
- Model / Reference
- 40240 FDA UDI
- Description
- 1 Each SUPER VIEW® Sterile Disposable HD Plus Lens Set for use with ZEISS RESIGHT® FDA UDI
Identifiers
- Catalog Number
- 40240 FDA UDI
- Primary DI / UDI-DI
- 00852475007042 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
Category: Ophthalmic diagnostic condensing lens
SUPER VIEW® Lens Set, HD Plus, Disposable for ZEISS RESIGHT® by Oculus Surgical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Ophthalmic diagnostic condensing lens.
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Cleared under the same submission
K051630 also covers:
- SUPER VIEW® Disposable Lens Set for RESIGHT® — INSIGHT INSTRUMENTS, INC.
- SUPER VIEW® Disposable Lens Set for ZEISS RESIGHT® — INSIGHT INSTRUMENTS, INC.
- Contact Lens, HD Professional, Cohen-Benner, "CBC" — OCULUS SURGICAL INC
- SUPER VIEW Lens, Disposable Contact, Tornambe — OCULUS SURGICAL INC
- SUPER VIEW® Disposable Lens Set — OCULUS SURGICAL INC
- SUPER VIEW® Disposable Lens Set, Pivot Plus — OCULUS SURGICAL INC
- SUPER VIEW® Lens, Disposable Contact, Hassan-Tornambe — OCULUS SURGICAL INC
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Oculus Surgical Inc
Sources (1)
- FDA UDI 14536717-e28e-449c-9801-aa3372697959 37 fields · synced May 30, 2026