FDA Device Intelligence
Home › MIZUHO CORPORATION › Sugita Keyhole Applier

Sugita Keyhole Applier

MIZUHO CORPORATION · Model 07-942-20 · UDI-DI 04946329061802

HCI Prescription
10
510(k) clearances
54
Adverse events
5
Recalls
10
Facilities

Description

Sugita Keyhole Applier, Straight 13cm Shaft Length for Mini Clips

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

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.