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Acuity PB550-Uv-24.0

by Eyekon Medical, Inc.

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 NumberM454PB550UVP2401 UDI-DI Date18 Sep 2015ListedStatusListed 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  • Withdrawn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
Acuity
Generic Name
Posterior-chamber intraocular lens, pseudophakic
Model / Reference
PB550-UV-24.0
Primary DI / UDI-DI
M454PB550UVP2401
PMA Number
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

Cleared under the same submission (P880072)

Show all (12)

Other devices from Eyekon Medical, Inc.

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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