LC16

by Lenstec Barbados Inc

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 8 Jun 2026. What this means

Regulatory status

as of registry sync 8 Jun 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00844369018944 UDI-DI	Date6 May 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Intraocular lens-insertion cartridge
Model / reference: LC16

Primary DI / UDI-DI: 00844369018944
FDA product code: MSS
GMDN term: Intraocular lens-insertion cartridge

Device class: Class I
Regulation number: 886.4300
GUDID distribution status: In Commercial Distribution

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Class III
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See all devices from Lenstec Barbados Inc →

Properties

Supplied sterile
Single use
Lot / batch number
Serial number
Expiration date

Other properties (10)

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