enVista® Toric IOL ETE

by Bausch & Lomb Incorporated 441 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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10757770611239 UDI-DI	Date16 May 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: enVista® Toric IOL
Generic Name: Posterior-chamber intraocular lens, pseudophakic
Model / Ref / Catalog: ETE, ETEU125+255

Primary DI / UDI-DI: 10757770611239
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

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Properties

Sterile
Single Use
Implantable
Prescription Use
Lot / Batch Number
Serial Number
Expiration Date
Manufacturing Date

Other properties (6)

Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No