# Guilin Refine Medical Instrument Co., Ltd.

- Location (FDA's records): Guilin, CN
- FDA decisions: 3 (2023–2026): 3 510(k) clearances
- Product codes: EHD (1), EBZ (1), ELC (1)
- 510(k) review time since 2016: median 258 days, against 255 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Changzhou Sifary Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/changzhou-sifary-medical-technology)
- DiaDent Group International: 1 (https://510kreport.com/company/diadent-group-international)
- San Diego Swiss Machining, Inc.: 1 (https://510kreport.com/company/san-diego-swiss-machining)

## Recent decisions
- K254018: Portable Dental X-ray Device (GT-1) (Feb 19, 2026)
- K230641: Ultrasonic Scaler Tips (Nov 21, 2023)
- K223414: Curing Light, Model: MaxCure 9 (Nov 15, 2023)

Source page: https://510kreport.com/company/guilin-refine-medical-instrument