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Titanium Nucleus Splitter 5512

by Katalyst Surgical, LLC

Titanium Nucleus Splitter 5512 is a Class I device made by Katalyst Surgical, LLC, listed in FDA GUDID since 20 Jun 2019 (UDI-DI 00840096202151), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840096202151 UDI-DI Date20 Jun 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Titanium Nucleus Splitter
Generic name
Ophthalmic surgical probe, reusable
Model / reference
5512
Primary DI / UDI-DI
00840096202151
FDA product code
HNQ
GMDN term
Ophthalmic surgical probe, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Ophthalmic surgical probe, reusable

Other devices from Katalyst Surgical, LLC

See all devices from Katalyst Surgical, LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)