Titanium Corneal Epithelium Spatula

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name: Titanium Corneal Epithelium Spatula FDA UDI
Generic Name: Ophthalmic surgical probe, reusable FDA UDI
Device Name: Titanium Corneal Epithelium Spatula FDA UDI
Model / Reference: 8085 FDA UDI
Description: Titanium Corneal Epithelium Spatula FDA UDI

Identifiers

Primary DI / UDI-DI: 00840096207354 FDA UDI
FDA Product Code: HMX FDA UDI
GMDN Term: Ophthalmic surgical probe, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic surgical probe, reusable

Titanium Corneal Epithelium Spatula by Katalyst Surgical, Llc — 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: Katalyst Surgical, Llc

Sources (1)

FDA UDI d4a782bb-f0ba-42e6-8919-6ada4a1b3ea3 33 fields · synced Jun 1, 2026