SureFine Pen Needle

FDA 510(k) K152877 · Shina Med Corporation

Substantially Equivalent

510(k) numberK152877

Submission

Device name
SureFine Pen Needle
Applicant
Shina Med Corporation
Anseong-Si, KR
Received
September 30, 2015
Decision date
June 7, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMI – Needle, Hypodermic, Single Lumen
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5570
Specialty
General Hospital

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K254273Verisafe Safety Sterile Needles (SSN)FMI · Special Promisemed Hangzhou Meditech Co., Ltd.04/16/2026SE
K252908Easydrip Classic Pen Needle; Easydrip Plus Pen Needle; Easydrip Classic Pro Pen Needle…FMI · Special Sandstone Medical (Suzhou), Inc.03/25/2026SE
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More from Ningbo Medsun Medical Co., Ltd.

510(k)DeviceDecision
K250510Sure-Fine Insulin SyringesFMF · Special 10/15/2025SE
K250658SureFine Pen NeedleFMI · Special 04/03/2025SE
K231165Shina Syringe; Shina Safety SyringeMEG · Traditional 10/27/2023SE
K210848Sure-Fine Insulin SyringesFMF · Special 03/01/2022SE
K191531Sure-Fine Insulin SyringesFMF · Special 09/06/2019SE
K152879Sure-Fine Insulin SyringesFMF · Traditional 09/09/2016SE

Questions and answers

When was SureFine Pen Needle cleared by the FDA?

SureFine Pen Needle (K152877) received a 510(k) decision of Substantially Equivalent on June 7, 2016, 251 days after the submission was received.

What is the product code of K152877?

The FDA product code is FMI – Needle, Hypodermic, Single Lumen, a Class II (moderate risk) device regulated under 21 CFR 880.5570.