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AESCULAP

AESCULAP, INC. · Model TEK8084R-L · UDI-DI 04046955543748

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

Description

, non-sterile, reusable

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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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.