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LC24

by Lenstec Barbados Inc

LC24 is a Class I device made by Lenstec Barbados Inc, listed in FDA GUDID since 6 May 2024 (UDI-DI 00844369018968), registry data as of 1 Jun 2026.

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

Source GUDID, synced 1 Jun 2026.

Regulatory status

as of registry sync 1 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00844369018968 UDI-DI Date6 May 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Intraocular lens-insertion cartridge
Model / reference
LC24
Primary DI / UDI-DI
00844369018968
FDA product code
MSS
GMDN term
Intraocular lens-insertion cartridge
Device class
Class I
Regulation number
886.4300
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Intraocular lens-insertion cartridge.

Other devices from Lenstec Barbados Inc

See all devices from Lenstec Barbados Inc →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (10, all answered No)