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enVista Aspire™ Toric IOL ETA

by Bausch & Lomb Incorporated 513 variants

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

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 Number10757770625427 UDI-DI Date17 Nov 2023ListedStatusListed GUDID: 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  • Withdrawn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
enVista Aspire™ Toric IOL
Generic name
Posterior-chamber intraocular lens, pseudophakic
Model / Ref / Catalog
ETA, ETAU500+060
Primary DI / UDI-DI
10757770625427
FDA product code
HQL
GMDN term
Posterior-chamber intraocular lens, pseudophakic
Device class
Class III
Regulation number
886.3600
GUDID distribution status
In Commercial Distribution

Related devices

Category: Posterior-chamber intraocular lens, pseudophakic

Other devices from Bausch & Lomb Incorporated

See all devices from Bausch & Lomb Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date

Other properties (7)

  • Sterilise before use: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No