Identity
- Trade Name
- Anodyne Surgical FDA UDI
- Generic Name
- Ophthalmic knife, reusable FDA UDI
- Device Name
- 1.0mm Lancet LRI Diamond Knife, Preset 600 micron Aluminum Handle 4.75" Long FDA UDI
- Model / Reference
- KA9600 FDA UDI
- Description
- 1.0mm Lancet LRI Diamond Knife, Preset 600 micron Aluminum Handle 4.75" Long FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840516141268 FDA UDI
- FDA Product Code
- HNN FDA UDI
- GMDN Term
- Ophthalmic knife, reusable 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
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Ophthalmic knife, reusable
Anodyne Surgical by Psi/Eye-Ko, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic knife, reusable.
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- Ophthalmic Knife — Katena Products, Inc. · Class I
- Walcott Rx Products — Walcott Rx Product Inc · Class I
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- Wexler Surgical, Inc. — Wexler Surgical, Inc. · Class I
- Walcott Rx Products — Walcott Rx Product Inc · Class I
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
- Psi/Eye-Ko, Inc.
Sources (1)
- FDA UDI 86e1d694-3cae-4bea-8799-2955da6e2410 34 fields · synced May 30, 2026