# Gimbo Medical Technology Shenzhen Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 7 (2024–2026): 7 510(k) clearances
- Product codes: MQL (5), MQK (1), MQE (1)
- 510(k) review time since 2016: median 144 days, against 195 for FDA's reviews in the same codes and years (5 of 6 faster)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Casebioscience, Inc.: 1 (https://510kreport.com/company/casebioscience)

## Its most-cited devices
- K240149: Giftlife™ Fertilization Medium; Giftlife™ Cleavage Medium; Giftlife™ Blastocyst Medium; Giftlife™ Single Step Medium (2024), cited by 1

## Recent decisions
- K253121: Giftlife Single Lumen Oocyte Retrieval Needle, Giftlife Double Lumen Oocyte Retrieval Needle (Jun 15, 2026)
- K242043: Sperm Freezing Medium (Jan 8, 2025)
- K242968: Giftlife® Single-Step Medium Plus (Nov 22, 2024)
- K240002: G-Vitri™ Vitrification Straw (Jun 14, 2024)
- K240149: Giftlife™ Fertilization Medium; Giftlife™ Cleavage Medium; Giftlife™ Blastocyst Medium; Giftlife™ Single Step Medium (Jun 13, 2024)
- K234023: Oocyte Flushing & Retrieval Medium; Gamete Buffer (May 10, 2024)
- K232942: G-Vitri™ Vitrification Freeze Media; G-Vitri™ Vitrification Thawing Media (Jan 30, 2024)

Source page: https://510kreport.com/company/gimbo-medical-technology-shenzhen