Identity
- Trade Name
- 20ga Bending Laser Probe - Alcon Compatible FDA UDI
- Generic Name
- Ophthalmic laser system beam guide FDA UDI
- Device Name
- 20ga Bending Laser Probe - Alcon Compatible FDA UDI
- Model / Reference
- VS0140.20A FDA UDI
- Description
- 20ga Bending Laser Probe - Alcon Compatible FDA UDI
Identifiers
- Catalog Number
- VS0140.20A FDA UDI
- Primary DI / UDI-DI
- B384VS014020A1 FDA UDI
- 510(k) Number
- K142830 FDA UDI
- FDA Product Code
- HQB FDA UDI
- GMDN Term
- Ophthalmic laser system beam guide FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4690 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
No
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
- Needle Gauge — 20 Gauge FDA UDI
Category: Ophthalmic laser system beam guide
20ga Bending Laser Probe - Alcon Compatible by Vortex Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Ophthalmic laser system beam guide.
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- OtoProbe™ Short Angled Box of 6 — Iridex Corporation · Class II
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
- Vortex Surgical, Inc.
Sources (1)
- FDA UDI e301975b-78ea-4d33-b815-b53817b57889 37 fields · synced May 31, 2026