# Guilin Kevin Peter Technology Co., Ltd.

- Location (FDA's records): Guilin, CN
- FDA decisions: 4 (2026–2026): 4 510(k) clearances
- Product codes: KIF (2), GEX (1), EBF (1)
- 510(k) review time since 2016: median 106 days, against 99 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 6 (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
- Meta Biomed Co., Ltd.: 1 (https://510kreport.com/company/meta-biomed)
- Ivoclar Vivadent, Inc.: 1 (https://510kreport.com/company/ivoclar-vivadent)
- Hulaser, Inc.: 1 (https://510kreport.com/company/hulaser)
- Biolase, Inc.: 1 (https://510kreport.com/company/biolase)
- 3M Company Espe Dental Products: 1 (https://510kreport.com/company/3m-company-espe-dental-products)
- Innovative Bioceramix, Inc.: 1 (https://510kreport.com/company/innovative-bioceramix)

## Recent decisions
- K261047: Dental Diode Laser Device (Laser-Pen) (Sep 18, 2026)
- K261695: Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF) (Aug 31, 2026)
- K261514: Calcium Hydroxide Temporary Filling Material (KP-Cal) (Aug 25, 2026)
- K261415: Injectable Root Canal Sealer (KP-Root SP) (Jun 29, 2026)

Source page: https://510kreport.com/company/guilin-kevin-peter-technology