FDA applicant
Nantong Holycon Medical Devices Co., Ltd.
FDA records 1 decision for Nantong Holycon Medical Devices Co., Ltd. (Nantong, CN) in 2017: 1 510(k) clearance. All are in product code GAM (Suture, Absorbable, Synthetic, Polyglycolic Acid). Its devices cite 1 predicate, 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 Nantong Holycon Medical Devices Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2017
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
Planning a device like Nantong Holycon Medical Devices Co.…’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 “Nantong”
FDA records each applicant name separately; these may or may not be the same firm.