510(k) K252906

ECHELON ENDOPATH Staple Line Reinforcement (ECH60R) by Ethicon Endo-Surgery, LLC — Product Code OXC

K252906 is an FDA 510(k) premarket notification submitted by Ethicon Endo-Surgery, LLC for the device "ECHELON ENDOPATH Staple Line Reinforcement (ECH60R)". The FDA issued a decision of Substantially Equivalent on January 9, 2026. The device falls under product code OXC (Mesh, Surgical, Absorbable, Staple Line Reinforcement), a Class II device regulated under 21 CFR 878.3300. Ethicon Endo-Surgery, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 9, 2026
Date Received
September 12, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mesh, Surgical, Absorbable, Staple Line Reinforcement
Device Class
Class II
Regulation Number
878.3300
Review Panel
SU
Submission Type

For reinforcement of soft tissue where weakness exists during staple line reinforcement procedures.