FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

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

K Number: K251062 · Decision Aug 14, 2025
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
56
Applicant Total
27
Review Days
132

Basic Information

Device Name
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
K Number
K251062
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Geistlich Pharma AG
Date Received
April 4, 2025
Decision Date
August 14, 2025
Product Code
NPL
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
NPL Barrier, Animal Source, Intraoral

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Other Clearances by Geistlich Pharma AG

K Number Device Name
K260364 Device 300419 Strip
K260532 Derma-Gide
K251323 Device 104 Particulate
K252253 Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide®
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 →