FDA 510(k) FDA unclassified Substantially Equivalent 🇨🇭 Switzerland

Derma-Gide

K Number: K260532 · Decision Mar 19, 2026
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
187
Applicant Total
27
Review Days
30

Basic Information

Device Name
Derma-Gide
K Number
K260532
Device Class
FDA unclassified
Clearance Type
Special
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Geistlich Pharma AG
Date Received
February 17, 2026
Decision Date
March 19, 2026
Product Code
KGN
Advisory Committee
Unknown
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
KGN Wound Dressing With Animal-Derived Material(S)

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Other Clearances by Geistlich Pharma AG

K Number Device Name
K260364 Device 300419 Strip
K251323 Device 104 Particulate
K252253 Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide®
K251062 Geistlich Bio-Gide; Geistlich Bio-Gide® Shape; Geistlich Bio-Gide® Compressed; Geistlich Bio-Gide® Forte; Geistlich Bio-Gide® Perio; Geistlich Combi-Kit Collagen®; Geistlich Perio-System Combi Pack
K251556 Device 300423 Granules
K251786 Geistlich Bio-Oss®; Geistlich Bio-Oss Pen®
K251613 SwissGraft X
K250833 SwissMembrane X; SwissMembrane X Socket
K242510 Geistlich Bio-Flow®
K241802 Device 300397 Putty
Search all 27 clearances from Geistlich Pharma AG →