FDA applicant
Guilin Kevin Peter Technology Co., Ltd.
FDA records 4 decisions for Guilin Kevin Peter Technology Co., Ltd. (Guilin, CN) in 2026: 4 510(k) clearances. Most are in product codes KIF (Resin, Root Canal Filling) and GEX (Powered Laser Surgical Instrument). Since 2016 its 510(k)s took a median of 106 days from receipt to decision, against 99 for FDA’s reviews in the same codes and years. Its devices cite 6 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Guilin Kevin Peter Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
4in 2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2026.
Planning a device like Guilin Kevin Peter Technology Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Guilin”
FDA records each applicant name separately; these may or may not be the same firm.