Depuy International, Ltd.
Depuy International, Ltd. has 0 FDA recalls, 4 inspections, 1 510(k) clearance and 0 compliance actions on record.
- Latest inspection
- May 29, 2026 · VAI
- Latest 510(k)
- Jun 16, 2022
Newer recall under related name Johnson And Johnson Surgical Vision: Jul 31, 2026, Z-3064-2026.
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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 | 4 | Oct 26, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Related names
| Name | Recalls | 510(k) | Inspections | Compliance | Most recent recall |
|---|---|---|---|---|---|
| Johnson And Johnson Surgical Vision | 18 | 4 | 9 | 0 | Jul 31, 2026 (Z-3064-2026) |
| Synthes (Usa) Products | 164 | 45 | 7 | 0 | Feb 25, 2026 (Z-1703-2026) |
| Cerenovus | 1 | 10 | 11 | 0 | Oct 2, 2025 (Z-0434-2026) |
| Ethicon Endo-Surgery | 54 | 184 | 8 | 0 | Sep 11, 2025 (Z-0147-2026) |
| Ethicon | 76 | 208 | 15 | 0 | Aug 15, 2025 (Z-2605-2025) |
| Johnson And Johnson Vision Care | 10 | 12 | 3 | 0 | Jun 12, 2025 (Z-2163-2025) |
| Ethicon Endo Surgery | 4 | 2 | 2 | 0 | Mar 7, 2025 (Z-1516-2025) |
| Biosense Webster | 33 | 76 | 7 | 0 | Jan 5, 2025 (Z-1205-2025) |
| Ethicon Sarl, A Johnson And Johnson | 2 | 0 | 2 | 0 | Jun 11, 2024 (Z-2407-2024) |
| Depuy Orthopaedics | 155 | 210 | 11 | 2 | Mar 12, 2024 (Z-1456-2024) |
| Depuy Spine | 36 | 71 | 9 | 0 | May 20, 2022 (Z-1324-2022) |
| Janssen Pharmaceuticals | 4 | 0 | 31 | 2 | Oct 23, 2018 (D-0218-2019) |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| May 29, 2026 | Leeds, United Kingdom | Devices | Voluntary Action Indicated (VAI) | 1000199976 |
| May 26, 2017 | Leeds, United Kingdom | Devices | No Action Indicated (NAI) | 1000199976 |
| Jun 25, 2015 | Leeds, United Kingdom | Devices | Voluntary Action Indicated (VAI) | 1000199976 |
| Feb 16, 2012 | Leeds, United Kingdom | Devices | Voluntary Action Indicated (VAI) | 1000199976 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K201348 | DePuy 3D Additive TriFlange Acetabular Cup | Jun 16, 2022 |