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FINEVISION HP Trifocal IOL POD F GF +20.0 D

by Physiol

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number05414846625511 UDI-DI Date15 Dec 2025ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
FINEVISION HP Trifocal IOL
Generic Name
Posterior-chamber intraocular lens, pseudophakic
Model / Ref / Catalog
POD F GF +20.0 D, 36092200A
Primary DI / UDI-DI
05414846625511
PMA Number
FDA Product Code
HQL, MFK
GMDN Term
Posterior-chamber intraocular lens, pseudophakic
Device Class
Class III
Regulation Number
886.3600
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (P240038)

Show all (12)

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Properties

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

Other properties (7)

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