Ultra-Fast Warm
FDA 510(k) K260248 · Kitazato Corporation
510(k) numberK260248
Submission
- Device name
- Ultra-Fast Warm
- Applicant
- Kitazato Corporation
Fuji, JP - Received
- January 27, 2026
- Decision date
- April 28, 2026
- 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 |
| K252672 | CaseBio Culture w/HSA (CMH5); CaseBio Handling w/HSA (WHH5)MQL · Traditional | Casebioscience, Inc. | 02/20/2026SE |
| K250445 | Fast Warm - NXMQL · Traditional | Fujifilm Irvine Scientific | 09/12/2025SE |
| 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 |
|---|---|---|
| K251305 | Ultra-Fast Vitri; Ultra-Fast WarmMQL · Traditional | 08/26/2025SE |
| K200249 | Sequential Culture Media (Fertilization Medium [without HSA/rHA, with HSA, with rHA]…MQL · Traditional | 10/23/2020SE |
| K193522 | iMedium Single Step; iMedium Single Step with HSA; iMedium Single Step with rHAMQL · Traditional | 08/25/2020SE |
| K192845 | Sperm Freeze, Sperm FridgeMQL · Traditional | 08/17/2020SE |
| K192540 | Kitazato ET CathetersMQF · Traditional | 05/01/2020SE |
| K190199 | SepaSperm Washing Solution, SepaSperm SolutionMQL · Traditional | 09/26/2019SE |
| K181469 | Cryotop®US-flash and Cryotop®US-scoopMQK · Traditional | 11/09/2018SE |
| K182002 | Cumulus RemoverMQL · Traditional | 10/23/2018SE |
| K171748 | Vitrification Kit and Thawing KitMQL · Traditional | 12/14/2017SE |
| K162878 | Kitazato ET CathetersMQF · Traditional | 07/13/2017SE |
Questions and answers
When was Ultra-Fast Warm cleared by the FDA?
Ultra-Fast Warm (K260248) received a 510(k) decision of Substantially Equivalent on April 28, 2026, 91 days after the submission was received.
What is the product code of K260248?
The FDA product code is MQL – Media, Reproductive, a Class II (moderate risk) device regulated under 21 CFR 884.6180.