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Titanium Chalazion Curette, Double Ended, 1.5mm and 2.0mm

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Titanium Chalazion Curette, Double Ended, 1.5mm and 2.0mm FDA UDI
Generic Name
Ophthalmic curette, reusable FDA UDI
Model / Reference
1700-1520D FDA UDI

Identifiers

Primary DI / UDI-DI
00840096205985 FDA UDI
FDA Product Code
FZS FDA UDI
GMDN Term
Ophthalmic curette, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic curette, reusable

Titanium Chalazion Curette, Double Ended, 1.5mm and 2.0mm by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic curette, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 470cdbc0-fae3-4ccd-9a61-576974811730 32 fields · synced May 30, 2026