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Applier, Aneurysm Clip
FDA product code HCI · Class 2 · Neurology
578
Registered devices
54
Adverse events
5
Recalls
14
510(k) clearances
Devices with this code
AESCULAP — AESCULAP, INC.LAZIC — Peter Lazic GmbHSUGITA ANEURYSM CLIP — MIZUHO CORPORATIONLAZIC — Peter Lazic GmbHAESCULAP — Aesculap AGLAZIC — Peter Lazic GmbHCODMAN — Cerenovus, Inc.AESCULAP — Aesculap AGAESCULAP — AESCULAP, INC.Sugita Keyhole Applier — MIZUHO CORPORATIONLAZIC — Peter Lazic GmbHSUGITA ANEURYSM CLIP — MIZUHO CORPORATIONSUGITA ANEURYSM CLIP — MIZUHO CORPORATIONSugita AVM Micro Clip Single Shaft Applier — MIZUHO CORPORATIONLAZIC — Peter Lazic GmbHSugita Titanium Clip II Applier — MIZUHO CORPORATIONLAZIC — Peter Lazic GmbHNOIR — Aesculap AGFukushima Keyhole Clip Applier — MIZUHO CORPORATIONSugita Titanium Clip II Applier — MIZUHO CORPORATIONLAZIC — Peter Lazic GmbHAESCULAP — AESCULAP, INC.Sugita Keyhole Applier — MIZUHO CORPORATIONSano Double Action Clip Applier — MIZUHO CORPORATION
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-10-06 | Peter Lazic Gmbh | Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. |
| 2023-10-06 | Peter Lazic Gmbh | Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. |
| 2023-10-06 | Peter Lazic Gmbh | Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip. |
| 2007-11-01 | Aesculap Inc | Breakage: the inner rod of the applier may corrode and break |
| 2007-11-01 | Aesculap Inc | Breakage: the inner rod of the applier may corrode and break |
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