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23ga Straight Illuminated Laser Probe, 19ga Needle Illumination, Iridex

FDA UDI

Class II (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
23ga Straight Illuminated Laser Probe, 19ga Needle Illumination, Iridex FDA UDI
Generic Name
Ophthalmic fibreoptic light instrument, single-use FDA UDI
Device Name
23ga Straight Illuminated Laser Probe, 19ga Needle Illumination, Iridex FDA UDI
Model / Reference
V6300-23AR FDA UDI
Description
23ga Straight Illuminated Laser Probe, 19ga Needle Illumination, Iridex FDA UDI

Identifiers

Primary DI / UDI-DI
10817489023614 FDA UDI
510(k) Number
K121187 FDA UDI
FDA Product Code
HQF FDA UDI
GMDN Term
Ophthalmic fibreoptic light instrument, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4390 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

23ga Straight Illuminated Laser Probe, 19ga Needle Illumination, Iridex by Katalyst Surgical, Llc — Class II — FDA UDI — listed in FDA GUDID

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ceccebf-dfa2-492e-95d7-752b218cb829 35 fields · synced May 30, 2026