Gunze Limited
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest FDA decision2022-08-26
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K221487 | NEOVEIL Staple Line Reinforcement | OXC | 2022-08-26 | View |
| 510(k) | K213498 | PELNAC Meshed Bilayer Wound Matrix | KGN | 2022-07-14 | View |
| 510(k) | K213573 | PELNAC Wound Matrix | KGN | 2022-02-09 | View |
| 510(k) | K191992 | PELNAC Bilayer Wound Matrix | KGN | 2020-04-29 | View |
No matching devices.