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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 AGSUGITA ANEURYSM CLIP — MIZUHO CORPORATIONLAZIC — Peter Lazic GmbHSUGITA ANEURYSM CLIP — MIZUHO CORPORATIONLAZIC — Peter Lazic GmbHLAZIC — Peter Lazic GmbHAESCULAP — Aesculap AGLAZIC — Peter Lazic GmbHAESCULAP — Aesculap AGSugita Titanium Clip II Single Shaft Applier — MIZUHO CORPORATIONAESCULAP — AESCULAP, INC.AESCULAP — AESCULAP, INC.NOIR — Aesculap AGAESCULAP — AESCULAP, INC.SUGITA BOOSTER CLIP — MIZUHO CORPORATIONAESCULAP — Aesculap AGFukushima Keyhole Clip Applier — MIZUHO CORPORATIONSUGITA ANEURYSM CLIP — MIZUHO CORPORATIONSugita Clip Remover — MIZUHO CORPORATIONSUGITA ANEURYSM CLIP — MIZUHO CORPORATIONSUGITA ANEURYSM CLIP — MIZUHO CORPORATIONSugita Keyhole Applier — MIZUHO CORPORATIONSugita Titanium Clip II Single Shaft Applier — MIZUHO CORPORATIONSugita AVM Microclip II Single Shaft Applier — MIZUHO CORPORATION

Recent recalls

DateFirmReason
2023-10-06Peter Lazic GmbhCustomer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
2023-10-06Peter Lazic GmbhCustomer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
2023-10-06Peter Lazic GmbhCustomer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
2007-11-01Aesculap IncBreakage: the inner rod of the applier may corrode and break
2007-11-01Aesculap IncBreakage: the inner rod of the applier may corrode and break

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.