Identity
- Trade Name
- Goniotome Handpiece FDA UDI
- Generic Name
- Ophthalmic knife, single-use FDA UDI
- Device Name
- The Handpiece is a sterile single use ophthalmic knife. It consists of a pencil-like instrument with a graspable white ABS plastic outer shell (~1.5 cm diameter and ~13 cm length), and a stainless steel probe (protruding about 2.2 cm from the tip of the white outer shell and covered by a protective purge chamber). The diameter of the probe insertable into the eye is ~1.1 mm. The tip of the probe features a pointed footplate tip and dual sharpened edges fabricated of stainless steel. The Handpiece is intended to be used in ophthalmic surgery to manually cut Trabecular Meshwork (TM) in adult and infantile patients. FDA UDI
- Model / Reference
- 550052-15 FDA UDI
- Description
- The Handpiece is a sterile single use ophthalmic knife. It consists of a pencil-like instrument with a graspable white ABS plastic outer shell (~1.5 cm diameter and ~13 cm length), and a stainless steel probe (protruding about 2.2 cm from the tip of the white outer shell and covered by a protective purge chamber). The diameter of the probe insertable into the eye is ~1.1 mm. The tip of the probe features a pointed footplate tip and dual sharpened edges fabricated of stainless steel. The Handpiece is intended to be used in ophthalmic surgery to manually cut Trabecular Meshwork (TM) in adult and infantile patients. FDA UDI
Identifiers
- Catalog Number
- 550052-15 FDA UDI
- Primary DI / UDI-DI
- 00854028002184 FDA UDI
- FDA Product Code
- HNN FDA UDI
- GMDN Term
- Ophthalmic knife, 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 knife, single-use
Goniotome Handpiece by Neomedix Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic knife, single-use.
- MANI Ophthalmic Knife — MANI, INC. · Class I
- Ophthalmic Knife — Katena Products, Inc. · Class I
- MANI Ophthalmic Knife — MANI, INC. · Class I
- MANI Ophthalmic Knife — MANI, INC. · Class I
- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- MANI Ophthalmic Knife — MANI, INC. · Class I
- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
- MANI Ophthalmic Knife — MANI, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Neomedix Corp.
Sources (1)
- FDA UDI fe9c4643-5e00-476c-9a8a-28728cbf5c03 34 fields · synced May 31, 2026