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Healon Ultimate Dual Pack 10290060

by Johnson & Johnson Surgical Vision, Inc.

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00385445402214 UDI-DI Date14 Nov 2014ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Healon Ultimate Dual Pack
Generic Name
Vitreous/aqueous humour replacement medium, intraoperative
Model / Ref / Catalog
10290060
Primary DI / UDI-DI
00385445402214
FDA Product Code
LZP
GMDN Term
Vitreous/aqueous humour replacement medium, intraoperative
Device Class
Class III
Regulation Number
886.4275
GUDID distribution status
Not in Commercial Distribution

Other devices from Johnson & Johnson Surgical Vision, Inc.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No