HomeUSACollagen Matrix, Inc.

Collagen Matrix, Inc.

USA · Oakland
✓ Record-verifiedregistrations found in 9 markets

This company has registrations in United States, Brazil, Canada, Taiwan, Singapore, Australia, Hong Kong, Israel, Russia — 9 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
14listed device types
Class I 1Class II 12Class III 0unclassified 1
plus 141 registration records and 47 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
9 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
20 including historic records
TWTaiwanTFDA
18valid device licences
Class II 18
SGSingaporeHSA SMDR
3device registrations
CLASS D 3
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
34active ARTG entries
Class III 34
HKHong KongMDACS
1valid listings
Class IV 1
ILIsraelAMAR
21registrations
RURussiaRoszdravnadzor
5active registrations
Class 3 5
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States141 registration records, 47 510(k), 0 PMA, 4 excluded
Manufacturer names merged into this page: Collagen Matrix, Inc. · COLLAGEN MATRIX, INC. · Collagen Matrix, Inc · COLLAGEN MATRIX INC · COLLAGEN MATRIX, INC

Company information

Country
USA
City
Oakland

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

52004
22005
52006
22007
12008
22009
22010
12011
12012
42014
22015
12016
42017
12019
12020
12021
22022
12023
42024
12025

FDA listed device types

showing 8 of 14
Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon 1Filler, Bone Void, Calcium Compound 1Bone Grafting Material, Animal Source 1Dura Substitute 1Barrier, Animal Source, Intraoral 1Barrier, Synthetic, Intraoral 1Mesh, Surgical 1Mesh, Surgical, Deployer 1

Registration details (sample)

MarketIdentifierNameClass / date
USK251191Collagen Dura Regeneration Membrane - Repair2025-11-18
USK243071Bovine Dermis Collagen Dermal Matrix2024-12-19
USK242302RejuvaKnee™ Collagen Meniscus Implant2024-10-02

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