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SurgiWrap®

MAST BIOSURGERY USA INC. · Model 180 x 280 x 0.02mm · UDI-DI 08964050272065

FTL Prescription
1
510(k) clearances
170,261
Adverse events (862 deaths)
73
Recalls
140
Facilities

Description

Bioresorbable protective sheet made from polylactide: a copolymer of 70:30 Poly(L-lactide-co-D,L-lactide). To be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological or gastroenterological anatomy or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. Minimizes tissue attachments to the device in case of direct contact with the viscera. Indicated for open and laparoscopic procedures.

Recalls

DateFirmReason
2024-07-03W.L. Gore & Associates, Inc.Devices were labeled with an expiration date of four years and ten days rather than the validated two years.
2023-04-25Davol, Inc.Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequa
2023-04-25Davol, Inc.Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequa
2023-04-25Davol, Inc.Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequa
2023-04-25Davol, Inc.Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequa
2023-01-11Covidien, LPCollagen film was placed on the opposite side of the mesh may cause delay to treatment/therapy, adhesions, erosion/migration, pain, fistula, hernia (recurrence), and failure of imp
2022-08-12Chamberlain Technologies LLCPotential presence of residual adhesive material on the mesh surface.
2022-08-12Chamberlain Technologies LLCPotential presence of residual adhesive material on the mesh surface.
2022-08-12Chamberlain Technologies LLCPotential presence of residual adhesive material on the mesh surface.
2022-08-12Chamberlain Technologies LLCPotential presence of residual adhesive material on the mesh surface.

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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.