FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™ Technology; Endo GIA™ Gray Articulating Reloads; Signia™ Small Diameter Reloads

K Number: K253657 · Decision Apr 10, 2026
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
282
Applicant Total
2
Review Days
141

Basic Information

Device Name
Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™ Technology; Endo GIA™ Gray Articulating Reloads; Signia™ Small Diameter Reloads
K Number
K253657
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4750
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Covidien (Part of Medtronic)
Date Received
November 20, 2025
Decision Date
April 10, 2026
Product Code
GDW
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GDW Staple, Implantable

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