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TenSURE

ATRICURE, INC. · Model 7 lb · UDI-DI 00818354017618

FZT Prescription
10
510(k) clearances
609
Adverse events
6
Recalls
255
Facilities

Description

A sterile, manual, hand-held surgical device intended for controlled tightening of a ligature loop in situ (e.g., during vascular surgery). The ligature is intended to be loaded into the device, which typically includes a sliding mechanism, allowing controlled manual tightening; the device may also include tightening markers. This is a single-use device

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2010-06-04Maquet CardiovascularPouch integrity may be compromised, resulting in loss of sterility.
2008-04-24Ethicon Endo-Surgery IncThe firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.
2008-04-24Ethicon Endo-Surgery IncThe firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.
2008-04-24Ethicon Endo-Surgery IncThe firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.
2008-04-24Ethicon Endo-Surgery IncThe firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.

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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.