MiniLoad Syringe
FDA 510(k) K212544 · Ocuject, LLC
510(k) numberK212544
Submission
- Device name
- MiniLoad Syringe
- Applicant
- Ocuject, LLC
Newport Beach, CA, US - Received
- August 12, 2021
- Decision date
- October 13, 2021
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
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) | Device | Applicant | Decision |
|---|---|---|---|
| K262581 | GraftGun Universal Graft Delivery System (GDS®)FMF · Special | SurGenTec, LLC | 08/26/2026SE |
| K252184 | SOL-M Luer Lock Syringe with Exchangeable Needle TrayFMF · Traditional | Sol-Millennium Medical, Inc. | 08/25/2026SE |
| K253747 | Disposable Pen Injector (KXYC-03C02, KXYC-03A03)FMF · Traditional | Jiangsu Enjosim Medical Technology Co., Ltd. | 08/14/2026SE |
| K260208 | Ultra-Fine SAFETY Insulin SyringeFMF · Traditional | embecta Medical II, LLC | 07/13/2026SE |
| K253110 | Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeFMF · Traditional | Sol-Millennium Medical, Inc. | 06/18/2026SE |
| K260514 | Profoject Safety Needle; Profoject Syringe with Safety Needle; Profoject Low Dead…FMF · Traditional | CMT Health PTE., Ltd. | 06/12/2026SE |
| K253112 | Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec…FMF · Special | Hlb Lifescience Co., Ltd. | 05/21/2026SE |
| K252279 | Sterile Hypodermic Syringe for Single Use (20ml, 30ml, 50ml, 60ml)FMF · Traditional | Chirana T.Injecta,A.S. | 04/17/2026SE |
| K253068 | Profoject Insulin Syringes; Profoject Safelock Disposable Insulin SyringeFMF · Traditional | CMT Health PTE., Ltd. | 02/23/2026SE |
| K253769 | Instylla Delivery KitFMF · Special | Instylla, Inc. | 12/22/2025SE |
More from Instylla, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K242956 | LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety NeedleQNS · Special | 10/25/2024SE |
| K233343 | SteriCap Safety Needle; VitreJect Safety NeedleFMI · Abbreviated | 11/27/2023SE |
| K230959 | VitreJect® Needle; OcuSafe® NeedleFMI · Traditional | 09/14/2023SE |
| K230372 | VitreJect SyringeQLY · Traditional | 09/08/2023SE |
| K212805 | SteriCap Mini Needle and Standard NeedlesFMI · Special | 09/30/2021SE |
| K202432 | MiniLoad SyringeFMF · Traditional | 02/19/2021SE |
| K170768 | Mini NeedleFMI · Traditional | 07/10/2017SE |
Questions and answers
When was MiniLoad Syringe cleared by the FDA?
MiniLoad Syringe (K212544) received a 510(k) decision of Substantially Equivalent on October 13, 2021, 62 days after the submission was received.
What is the product code of K212544?
The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.