Disposable Pen Injector (KXYC-03C02, KXYC-03A03)

FDA 510(k) K253747 · Jiangsu Enjosim Medical Technology Co., Ltd.

Substantially Equivalent

510(k) numberK253747

Submission

Device name
Disposable Pen Injector (KXYC-03C02, KXYC-03A03)
Applicant
Jiangsu Enjosim Medical Technology Co., Ltd.
Wu Xi, CN
Received
November 25, 2025
Decision date
August 14, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

Other 510(k)s with product code FMF

510(k)DeviceApplicantDecision
K262581GraftGun Universal Graft Delivery System (GDS®)FMF · Special SurGenTec, LLC08/26/2026SE
K252184SOL-M Luer Lock Syringe with Exchangeable Needle TrayFMF · Traditional Sol-Millennium Medical, Inc.08/25/2026SE
K260208Ultra-Fine™ SAFETY Insulin SyringeFMF · Traditional embecta Medical II, LLC07/13/2026SE
K253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeFMF · Traditional Sol-Millennium Medical, Inc.06/18/2026SE
K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead…FMF · Traditional CMT Health PTE., Ltd.06/12/2026SE
K253112Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec…FMF · Special Hlb Lifescience Co., Ltd.05/21/2026SE
K252279Sterile Hypodermic Syringe for Single Use (20ml, 30ml, 50ml, 60ml)FMF · Traditional Chirana T.Injecta,A.S.04/17/2026SE
K253068Profoject™ Insulin Syringes; Profoject™ Safelock Disposable Insulin SyringeFMF · Traditional CMT Health PTE., Ltd.02/23/2026SE
K253769Instylla Delivery KitFMF · Special Instylla, Inc.12/22/2025SE
K252518DuoprossTM Smart Cap (Type I)FMF · Traditional Duopross Meditech Corporate12/17/2025SE

Questions and answers

When was Disposable Pen Injector (KXYC-03C02, KXYC-03A03) cleared by the FDA?

Disposable Pen Injector (KXYC-03C02, KXYC-03A03) (K253747) received a 510(k) decision of Substantially Equivalent on August 14, 2026, 262 days after the submission was received.

What is the product code of K253747?

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