Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Mirco-Tech (Nanjing) Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 29, 2026: Injection Needle.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 29, 2026 | Injection NeedleK260262 · FBK | 510(k) clearances |
| Apr 24, 2026 | Dilation Balloon CatheterK253832 · FGE | 510(k) clearances |
| Apr 3, 2026 | Single-use Video Scope; PB Digital ControllerK254153 · FBN | 510(k) clearances |
| Mar 19, 2026 | Disposable Distal CapK253139 · FBN | 510(k) clearances |
| Mar 19, 2024 | Disposable Dual Action Tissue Closure DeviceK233772 · PKL | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
