510(k) K253956

Device
ProGrip™ advanced self-gripping polypropylene mesh (ADG1510, ADG2015, ADG3020, ADG4030)
Applicant
Sofradim Production
510(k) number
K253956
Product code
FTL
Decision
Substantially Equivalent (SESE)
Decision date
2026-05-21
Date received
2025-12-10
Regulation
878.3300
Classification name
Mesh, Surgical, Polymeric
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Anne Bertron
Address
116 Ave. Du Formans Trévoux FR 01600 01600

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code FTL

510(k)DeviceApplicantDecision date
K253125Parietene™ Flat Sheet MeshMedtronic - Sofradim Production2025-10-24
K251955Onflex™ MeshDavol Inc., Subsidiary of C. R. Bard, Inc.2025-07-24
K251557Bard® Mesh; Bard® Mesh Pre-ShapedDavol, Inc.2025-06-12
K250869Parietene™ Macroporous Mesh (PPM5050 )Sofradim Production2025-04-23
K250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedDavol, Inc.2025-04-09
K243315ProGrip™ Self-Gripping Polypropylene MeshSofradim Production2025-01-17
K2412503DMax Light MeshDavol Inc., Subsidiary of C. R. Bard, Inc.2024-06-14
K232373Progrip™ Self-Gripping Polypropylene MeshSofradim Production2024-01-18
K233402Bard 3DMax MeshDavol Inc., Subsidiary of C. R. Bard, Inc.2023-11-01
K232924T-Line® Hernia MeshDeep Blue Medical Advances, Inc.2023-10-18
K230671Pitch PaSoft Tissue Reinforcement DeviceXiros, Ltd.2023-05-31
K230227T-Line Hernia MeshDeep Blue Medical Advances, Inc.2023-02-23
K223218Parietene Macroporous MeshSofradim Production2022-12-02
K221556T-Line Hernia MeshDeep Blue Medical Advances, Inc.2022-11-28
K220540ProGrip Self-Gripping Polypropylene MeshCovidien2022-09-22