Gimbo Medical Technology Shenzhen Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242043 | Sperm Freezing Medium | January 8, 2025 |
| K242968 | Giftlife® Single-Step Medium Plus | November 22, 2024 |
| K240002 | G-Vitri Vitrification Straw | June 14, 2024 |
| K240149 | Giftlife Fertilization Medium; Giftlife Cleavage Medium; Giftlife Blastocyst Medium; Giftlife Si | June 13, 2024 |
| K234023 | Oocyte Flushing & Retrieval Medium; Gamete Buffer | May 10, 2024 |
| K232942 | G-Vitri Vitrification Freeze Media; G-Vitri Vitrification Thawing Media | January 30, 2024 |