StaClear Syringe (SC250AN); StaClear Syringe (SC250LS); StaClear Syringe (SC250LL)

FDA 510(k) K251849 · Staclear, Inc.

Substantially Equivalent

510(k) numberK251849

Submission

Device name
StaClear Syringe (SC250AN); StaClear Syringe (SC250LS); StaClear Syringe (SC250LL)
Applicant
Staclear, Inc.
Raleigh, NC, US
Received
June 16, 2025
Decision date
November 21, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QLY – Ophthalmic Syringe
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

An Ophthalmic Syringe is a piston syringe intended for intraocular injections. The device consists of a calibrated hollow barrel, a movable plunger, and may include a needle. The device should be used by health care professionals to perform injections into the eye.

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K243936StaClear Syringe (SC250AN); StaClear Syringe (SC250LS); StaClear Syringe (SC250LL)QLY · Special Staclear, Inc.04/03/2025SE
K243149Microliter Dosing Syringe (9, 20, 25, 37.5, 50 and 100 microliter models)QLY · Traditional Congruence Medical Solutions, LLC12/20/2024SE
K230372VitreJect SyringeQLY · Traditional Ocuject, LLC09/08/2023SE
K200242StaClear SyringeQLY · Traditional Tribofilm Research, Inc.07/27/2020SE

More from Tribofilm Research, Inc.

510(k)DeviceDecision
K243936StaClear Syringe (SC250AN); StaClear Syringe (SC250LS); StaClear Syringe (SC250LL)QLY · Special 04/03/2025SE

Questions and answers

When was StaClear Syringe (SC250AN); StaClear Syringe (SC250LS); StaClear Syringe (SC250LL) cleared by the FDA?

StaClear Syringe (SC250AN); StaClear Syringe (SC250LS); StaClear Syringe (SC250LL) (K251849) received a 510(k) decision of Substantially Equivalent on November 21, 2025, 158 days after the submission was received.

What is the product code of K251849?

The FDA product code is QLY – Ophthalmic Syringe, a Class II (moderate risk) device regulated under 21 CFR 880.5860.