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SOFTEC HD PLI SOFHDPLI+19.0D and PLITIP1645 Kit

by Lenstec Barbados Inc

Active United States. Also listed in GUDID (US).

PMA

Valid until

No expiry

PMA approval is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

PMA P090022

FDA submission, from GUDID

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00844369002479 UDI-DI Date1 Aug 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA PMAAPPR from GUDID Approved NumberP090022 Date12 Apr 2010DecidedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA PMA Active

Specification

GUDID

Trade name
Softec Hd Pli
Generic name
Posterior-chamber intraocular lens, pseudophakic
Model / Ref / Catalog
SOFHDPLI+19.0D and PLITIP1645 Kit, SOFTEC HD PLI
Primary DI / UDI-DI
00844369002479
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

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Properties

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

Other properties (8)

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