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Tecnis IOL ZCT225

by Johnson & Johnson Surgical Vision, Inc. 59 variants

Tecnis IOL ZCT225 (ZCT225U330) is a Class III device made by Johnson & Johnson Surgical Vision, Inc., listed in FDA GUDID since 30 Jun 2015 (UDI-DI 05050474552999), 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 Number05050474552999 UDI-DI Date30 Jun 2015ListedStatusListed 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  • Withdrawn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
Tecnis IOL
Generic name
Posterior-chamber intraocular lens, pseudophakic
Model / Ref / Catalog
ZCT225, ZCT225U330
Primary DI / UDI-DI
05050474552999
FDA product code
MJP
GMDN term
Posterior-chamber intraocular lens, pseudophakic
Device class
Class III
Regulation number
886.3600
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 13 Millimeter

Related devices

Category: Posterior-chamber intraocular lens, pseudophakic

Other devices from Johnson & Johnson Surgical Vision, Inc.

See all devices from Johnson & Johnson Surgical Vision, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Serial number
  • Expiration date
Other properties (9, all answered No)