Anrei Medical (Hangzhou) Co., Ltd.
Anrei Medical (Hangzhou) Co., Ltd. has 0 FDA recalls, 0 inspections, 6 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Mar 21, 2022
Reviewing Anrei Medical (Hangzhou) Co., Ltd. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or get Anrei Medical (Hangzhou) Co., Ltd.'s full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 6 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 26, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K212999 | Multi-Functional Electrosurgical Knife | Mar 21, 2022 |
| K210917 | Single Use Injection Needle | May 28, 2021 |
| K202987 | Rescue Pulmonary Grasping Forceps | Apr 29, 2021 |
| K210660 | Stone Retrieval Balloon Catheter | Apr 27, 2021 |
| K201771 | Single Use Rotatable and Repositionable Hemoclip | Oct 19, 2020 |
| K192048 | Single Use Endoscope Valves Set | May 14, 2020 |