Aesculap, Inc.
FDA 510(k) & PMA Approved Devices — 196 products
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Total Devices196
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K260044 | Ventricular Catheters, Thomale Catheter | JXG | 2026-10-02 | View |
| 510(k) | K242762 | Aesculap Aicon® Series Container System | KCT | 2025-05-13 | View |
| 510(k) | K242003 | XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set | JXG | 2024-12-16 | View |
| 510(k) | K223596 | SQ.line KERRISON | HAE | 2023-06-29 | View |
| 510(k) | K214041 | Aesculap AICON Container | KCT | 2022-12-30 | View |
| 510(k) | K211572 | Aesculap Slim Clip Applier | HCI | 2021-12-13 | View |
| 510(k) | K203739 | ELAN 4 Electro Motor System | HBE | 2021-08-24 | View |
| 510(k) | K202391 | DIR 800 | IZI | 2021-01-21 | View |
| 510(k) | K203461 | Aesculap Caiman 12 Seal and Cut Technology System | GEI | 2020-12-18 | View |
| 510(k) | K202938 | Aesculap Caiman 5 Seal and Cut Technology System | GEI | 2020-10-30 | View |
| 510(k) | K202124 | Aesculap PAS-Port Proximal Anastomosis System | FZP | 2020-09-02 | View |
| 510(k) | K200950 | Ventricular Catheter | JXG | 2020-05-08 | View |
| 510(k) | K192056 | JJ Series Container System | KCT | 2020-03-27 | View |
| 510(k) | K193582 | SterilContainer S2 System | KCT | 2020-03-17 | View |
| 510(k) | K192266 | M. Blue Adjustable Shunt System | JXG | 2019-11-21 | View |
| 510(k) | K183203 | ELAN 4 Tools | HBE | 2019-08-09 | View |
| 510(k) | K182414 | Aesculap® SterilContainer(TM) S2 System | KCT | 2019-07-05 | View |
| 510(k) | K190174 | Miethke Shunt System GAV 2.0 and SA 2.0 Valves | JXG | 2019-07-05 | View |
| 510(k) | K183180 | Caiman 5 Maryland | GEI | 2019-03-12 | View |
| 510(k) | K182527 | ELAN 4 Tools | HBE | 2019-01-19 | View |
No matching devices.
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