Fast Warm - NX
FDA 510(k) K250445 · Fujifilm Irvine Scientific
510(k) numberK250445
Submission
- Device name
- Fast Warm - NX
- Applicant
- Fujifilm Irvine Scientific
Santa Ana, CA, US - Received
- February 14, 2025
- Decision date
- September 12, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MQL – Media, Reproductive
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.6180
- Specialty
- Obstetrics/Gynecology
Other 510(k)s with product code MQL
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254261 | Vitrification Freeze Kit and Thawing Kit (CS-IVF-FK; CS-IVF-TK)MQL · Traditional | Cell Store (Beijing) Biotechnology Co., Ltd. | 08/28/2026SE |
| K260248 | Ultra-Fast WarmMQL · Traditional | Kitazato Corporation | 04/28/2026SE |
| K252672 | CaseBio Culture w/HSA (CMH5); CaseBio Handling w/HSA (WHH5)MQL · Traditional | Casebioscience, Inc. | 02/20/2026SE |
| K251637 | Dewin Reproductive Media (Dewin Gamete Buffer [with HSA and without HSA]; Dewin Follicle…MQL · Traditional | Donnevie Medical Technology (Shanghai) Co. , Ltd. | 08/27/2025SE |
| K251305 | Ultra-Fast Vitri; Ultra-Fast WarmMQL · Traditional | Kitazato Corporation | 08/26/2025SE |
| K242640 | FertiCult Flushing medium; FertiCult Flushing medium with phenol red and gentamicinMQL · Traditional | Fertipro NV | 05/30/2025SE |
| K242561 | Dewin Reproductive Media (Dewin Vitrification Kit, Dewin Thawing Kit)MQL · Traditional | Donnevie Medical Technology (Shanghai) Co. , Ltd. | 04/10/2025SE |
| K242089 | Vitrification Freeze Kit (RFD-0101) Vitrification Thaw Kit (RFD-0201, RFD-0202)MQL · Traditional | Jiangsu Ruifuda Medical Device Co., Ltd. | 04/10/2025SE |
| K242107 | CaseMONO Culture (CMON); CaseMONO w/HEPES (WHMO); CaseBioscience® HTF (HTFC)…MQL · Traditional | Casebioscience, Inc. | 03/21/2025SE |
| K241833 | V-GradMQL · Traditional | Vitromed GmbH | 03/21/2025SE |
More from Vitromed GmbH
| 510(k) | Device | Decision |
|---|---|---|
| K241341 | cryo-GO Vitrification DeviceMQK · Traditional | 09/26/2024SE |
| K233764 | SSS-NX (Serum Substitute Supplement-NX)MQL · Traditional | 04/24/2024SE |
| K231804 | PRIME-XV FreezIS DMSO-Free MDNDS · Abbreviated | 11/09/2023SE |
| K190152 | Vit Kit- Freeze NX and Vit Kit- Warm NXMQL · Traditional | 06/21/2019SE |
Questions and answers
When was Fast Warm - NX cleared by the FDA?
Fast Warm - NX (K250445) received a 510(k) decision of Substantially Equivalent on September 12, 2025, 210 days after the submission was received.
What is the product code of K250445?
The FDA product code is MQL – Media, Reproductive, a Class II (moderate risk) device regulated under 21 CFR 884.6180.