Identity
- Trade Name
- TearCare(R) Clearance Assistant PLUS FDA UDI
- Generic Name
- Ophthalmic curette, single-use FDA UDI
- Device Name
- TearCare Clearance Assistant PLUS FDA UDI
- Model / Reference
- FG 06950 FDA UDI
- Description
- TearCare Clearance Assistant PLUS FDA UDI
Identifiers
- Catalog Number
- 5-107 FDA UDI
- Primary DI / UDI-DI
- 00858027006389 FDA UDI
- FDA Product Code
- HNS FDA UDIHNZ FDA UDI
- GMDN Term
- Ophthalmic curette, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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
Yes
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 soft-tissue manipulation forceps, tweezers-like, single-useOphthalmic curette, single-use
TearCare(R) Clearance Assistant PLUS by Sight Sciences, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 80e3bda0-8ef2-44ef-aa0d-a3d9e16ec826 34 fields · synced Jun 9, 2026