Collagen Matrix, Inc. - FDA 510(k) Cleared Devices
47
Total
47
Cleared
0
Denied
Collagen Matrix, Inc. has 47 FDA 510(k) cleared medical devices. Based in Franklin Lakes, US.
Latest FDA clearance: Nov 2025. Active since 2001. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Collagen Matrix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Collagen Matrix, Inc.
47 devices
Cleared
Nov 18, 2025
Collagen Dura Regeneration Membrane - Repair
Neurology
215d
Cleared
Dec 19, 2024
Bovine Dermis Collagen Dermal Matrix
General & Plastic Surgery
83d
Cleared
Oct 02, 2024
RejuvaKnee™ Collagen Meniscus Implant
Orthopedic
58d
Cleared
May 01, 2024
Soft Tissue Augmentation Resorbable Matrix
Dental
216d
Cleared
Mar 12, 2024
Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix
Orthopedic
28d
Cleared
Aug 02, 2023
Mineral Collagen Composite Bioactive Extra Moldable
Orthopedic
33d
Cleared
Dec 20, 2022
Mineral Collagen Composite Bioactive Moldable
Orthopedic
188d
Cleared
May 31, 2022
Fibrillar Collagen Wound Dressing
General & Plastic Surgery
236d
Cleared
Apr 02, 2021
Porcine Mineral Collagen Composite
Dental
241d
Cleared
Sep 11, 2020
Porcine Mineral Collagen Composite Moldable
Dental
67d
Cleared
Mar 21, 2019
Mineral Collagen Composite Bioactive Moldable
Orthopedic
232d
Cleared
Oct 30, 2017
Anorganic Bone Mineral with Collagen in Delivery Applicator
Dental
209d
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