Sterile Hypodermic Needles for Single Use

FDA 510(k) K231720 · Wepon Medical Technology Co., Ltd.

Substantially Equivalent

510(k) numberK231720

Submission

Device name
Sterile Hypodermic Needles for Single Use
Applicant
Wepon Medical Technology Co., Ltd.
Wenling, CN
Received
June 13, 2023
Decision date
September 8, 2023
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

Other 510(k)s with product code FMI

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K260933Safety Sterile Hypodermic Needles (NR-S1816R, NR-S1916R, NR-S1925R, NR-S1938R…FMI · Traditional Hangzhou Qiantang Longyue Biotechnology Co., Ltd.08/07/2026SE
K261829Profoject™ Dual-Safety Pen NeedlesFMI · Traditional CMT Health PTE., Ltd.07/29/2026SE
K260739Profoject™ Pen Needles (Model A; Model B)FMI · Traditional CMT Health PTE., Ltd.07/15/2026SE
K260855Profoject™ Safety Pen NeedlesFMI · Traditional CMT Health PTE., Ltd.06/10/2026SE
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
K253047Pressone™FMI · Traditional Nipro Medical Corporation03/24/2026SE
K253622Safety Pen NeedleFMI · Traditional Ningbo Medsun Medical Co., Ltd.03/18/2026SE

More from Ningbo Medsun Medical Co., Ltd.

510(k)DeviceDecision
K231729Sterile syringes for single use with/without needleFMI · Traditional 09/08/2023SE
K231727Sterile Auto-Disable Syringes with/without Needle for Single UseFMF · Traditional 09/08/2023SE
K231723Sterile Safety Hypodermic Needles for Single UseFMI · Traditional 09/08/2023SE
K212299Medical Surgical MaskFXX · Traditional 01/04/2022SE

Questions and answers

When was Sterile Hypodermic Needles for Single Use cleared by the FDA?

Sterile Hypodermic Needles for Single Use (K231720) received a 510(k) decision of Substantially Equivalent on September 8, 2023, 87 days after the submission was received.

What is the product code of K231720?

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