FDA applicant
Anhui Lntco Medical Products Co., Ltd.
FDA records 1 decision for Anhui Lntco Medical Products Co., Ltd. (Huaibei City, CN) in 2020: 1 510(k) clearance. All are in product code LZA (Polymer Patient Examination Glove). 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 Anhui Lntco Medical Products Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2020
2020high 1 (2020) · low 0 (2021)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2020.
Planning a device like Anhui Lntco Medical Products 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) Report