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23ga Dex™ Curved ILM Forceps

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
23ga Dex™ Curved ILM Forceps FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, probe-like, single-use FDA UDI
Device Name
Box of 5, 23ga Dex™ Curved ILM Forceps FDA UDI
Model / Reference
DVF4010-23 FDA UDI
Description
Box of 5, 23ga Dex™ Curved ILM Forceps FDA UDI

Identifiers

Primary DI / UDI-DI
00817489021859 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, probe-like, 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic soft-tissue manipulation forceps, probe-like, single-use

23ga Dex™ Curved ILM Forceps by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue manipulation forceps, probe-like, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katalyst Surgical, Llc

Sources (1)

  • FDA UDI 34fe0c3e-5428-4801-9ce5-132e83a3b018 33 fields · synced May 30, 2026