Us Endoscopy
Us Endoscopy has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record.
- Latest 510(k)
- Oct 25, 2019
Reviewing Us Endoscopy 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 Us Endoscopy'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 | 1 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 25, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K192518 | Reusable Monopolar Active Cord | Oct 25, 2019 |