K260532

Derma-Gide

510(k) number
K260532
Device name
Derma-Gide
Applicant
Geistlich Pharma AG CH
Product code
KGN — Wound Dressing With Animal-Derived Material(S)
Decision date
2026-03-19
Date received
2026-02-17
Decision
Substantially Equivalent
Clearance type
Special
Advisory committee
Unknown
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain

Also available from FDA: K260532.pdf

Official FDA record: K260532
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.