Identity
- Trade Name
- OMNI(R) Surgical System (US) FDA UDI
- Generic Name
- Trabeculotome, single-use FDA UDI
- Device Name
- OMNI System for US in a single pack FDA UDI
- Model / Reference
- FG 06721 FDA UDI
- Description
- OMNI System for US in a single pack FDA UDI
Identifiers
- Catalog Number
- 1-102 FDA UDI
- Primary DI / UDI-DI
- 00858027006372 FDA UDI
- FDA Product Code
- HMZ FDA UDIMRH FDA UDI
- GMDN Term
- Trabeculotome, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI880.5725 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
No
FDA UDI
Category: Ophthalmic needle, single-useTrabeculotome, single-use
OMNI(R) Surgical System (US) by Sight Sciences, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Trabeculotome, single-use.
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- Sion Surgical Instrument — Sight Sciences, Inc. · Class I
- OMNI Surgical System — Sight Sciences, Inc. · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Sight Sciences, Inc.
Sources (1)
- FDA UDI a7344e55-8e6e-42af-add4-35f58cc618dc 34 fields · synced Jun 9, 2026