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COLLAGEN MATRIX, INC.

United States·US-MF-000015783

Last updated September 17, 2026

Information

Country: United States
Address: 15 Thornton Rd, Oakland, United States
Website: collagenmatrix.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: (877) 540-3258
PRRC Contact: Peggy Hansen
EUDAMED SRN: US-MF-000015783
FDA FEI Number: 3008817245
DUNS Number: 176262442

Catalogue (727)

Page 3 of 15

Device	Model / Reference	Registries	Class	Status
BoneSync BioActive	ABS-3400-10	FDA UDI	Class II	Active
BIA-GEN Bioactive	CS-MCCBA1006	FDA UDI	Class II	Active
VENADO Carbonate Apatite Block	4817-T68202	FDA UDI	Class II	Active
OsteoMaxx Plug	XA625	FDA UDI	Class II	Active
OssiMend® Bioactive	MCCBA025	FDA UDI	Class II	Active
OssiMend Bioactive Moldable	MCCBA1006	FDA UDI	Class II	Active
OssiMend® Bioactive \| Putty	MCCBAM025	FDA UDI	Class II	Active
TriOSS Bioactive Moldable	BA0506	FDA UDI	Class II	Active
Arthrex Nerve Conduit	ABS-2025C	FDA UDI	Class II	Active
OSTEO-Tape	OSTEOTAPE	FDA UDI	U	Active
Neodent® Membrane Flex™	NAMND070.010	FDA UDI	Class II	Active
PARASORB RESODONT Flex	RDC2030	FDA UDI	Class II	Active
DuraMatrix-Onlay Plus	DMOP33	FDA UDI	Class II	Active
PreservaRidge™ Plug	PRPREG	FDA UDI	Class II	Active
Cohealyx™	BDCDM55-5	FDA UDI	U	Active
VENADO Carbonate Apatite Block	4817-T68101	FDA UDI	Class II	Active
MinerOss XP	MINXP-CAN2.0SM	FDA UDI	Class II	Active
Arthrex Nerve Conduit	ABS-6025C	FDA UDI	Class II	Active
VENADO Carbonate Apatite Strip	4817-T122101	FDA UDI	Class II	Active
Plena Plug	SMCP1020	FDA UDI	Class II	Active
SynOss Putty	SMB100	FDA UDI	Class II	Active
MatrixDerm EXT	PDMX3040	FDA UDI	Class II	Active
DuraMend™	NDM13	FDA UDI	Class II	Active
PlatFORM CM Putty	CM68910	FDA UDI	Class II	Active
DuraMatrix Onlay	CDSLM22	FDA UDI	Class II	Active
MatrixDerm CAP	PDMC1216	FDA UDI	Class II	Active
Plena Flex	CDMPP1520	FDA UDI	Class II	Active
naturesQue MaxOss P	58493	FDA UDI	Class II	Active
MatrixFlex	CDMPP2030	FDA UDI	Class II	Active
Stratofuse	BA47-000010	FDA UDI	Class II	Active
StarDerm 9-12	SD2030	FDA UDI	Class II	Active
StarGraft Granules	SGG350	FDA UDI	Class II	Active
OssiMend® Bioactive	MCCBA2025	FDA UDI	Class II	Active
Arthrex Nerve Wrap	ABS-6025W	FDA UDI	Class II	Active
BoneSync BioActive	ABS-3400-05	FDA UDI	Class II	Active
RegenerOss Resorbable Xenograft	ROXR10	FDA UDI	Class II	Active
OssiMend Bioactive Moldable	MCCBA4025	FDA UDI	Class II	Active
Cohealyx™	BDCDM24	FDA UDI	U	Active
naturesQue MaxOss P	58489	FDA UDI	Class II	Active
OSTEO-Derm	OSTEOD30x40	FDA UDI	Class II	Active
CopiOs Extend	0190Z	FDA UDI	Class II	Active
Symbios	32310000	FDA UDI	Class II	Active
Opus™ BA Strip	71421220	FDA UDI	Class II	Active
NeoGen Collagen Firm	64055	FDA UDI	Class II	Active
OssiMend Putty	PS-MCCP05	FDA UDI	Class II	Active
Plena Medium	PDM2030	FDA UDI	Class II	Active
Neodent® Membrane Flex™	NAMND070.009	FDA UDI	Class II	Active
OssiMend® Bioactive \| Strip	MCCBA0506	FDA UDI	Class II	Active
naturesQue MaxOss P	58495	FDA UDI	Class II	Active
OssiMend® Bioactive \| Strip	MCCBA2025	FDA UDI	Class II	Active

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Authorities

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FDA Recalls (15)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Aug 3, 2022	Z-1777-2022	—	open, classified	The packaging may not be sealed, which could compromise sterility.
Dec 13, 2021	Z-0668-2022	—	terminated	Outer packaging (outer pouch) is not sealed compromising sterility and result in potential risk of patient infection, which could lead to revision surgery
Dec 13, 2021	Z-0669-2022	—	terminated	Outer packaging (outer pouch) is not sealed compromising sterility and result in potential risk of patient infection, which could lead to revision surgery
Nov 5, 2019	Z-0909-2020	—	terminated	The products may have been packaged with an incorrect Instructions for Use.
Nov 5, 2019	Z-0910-2020	—	terminated	The products may have been packaged with an incorrect Instructions for Use.
Nov 5, 2019	Z-0908-2020	—	terminated	The products may have been packaged with an incorrect Instructions for Use.
Nov 5, 2019	Z-0907-2020	—	terminated	The products may have been packaged with an incorrect Instructions for Use.
Nov 5, 2019	Z-0912-2020	—	terminated	The products may have been packaged with an incorrect Instructions for Use.
Nov 5, 2019	Z-0911-2020	—	terminated	The products may have been packaged with an incorrect Instructions for Use.
Mar 19, 2019	Z-1389-2019	—	terminated	Product was packaged in the wrong box; may have been placed inside a Neomem FLEXPLUS box instead of a Neomem box
Oct 30, 2018	Z-0752-2019	—	terminated	There is a possibility that the product labeled as 4.0cc volume may only contain 2.0cc volume and is therefore mislabeled.
Aug 16, 2018	Z-0414-2019	—	terminated	There is a possibility that the product was packaged in the wrong box. Specifically, the product may have been placed inside a BioMend box instead of a BioMend Extend box. The only difference between the two boxes is the product trade name. The label placed on the box and on the product packaged inside the box is correct. The Instructions for Use inside the box are correct.
Nov 17, 2015	Z-1173-2016	—	terminated	The distributor, Osteogenics Biomedical, notified the firm that the syringes were not working properly and the syringes were being held in quarantine.
Aug 25, 2015	Z-1096-2016	—	terminated	On 8/25/2015, Collagen Matrix, Inc discovered that one of the 171 units of NuOss Cancellous product shipped to a distributor may have included an incorrect size.
May 13, 2013	Z-1097-2016	—	terminated	During the 36 month real time shelf life testing of NuOss XC Sinus (BMCU-Umbrella) to verify the 3 year shelf life designated for the device, 3 of 13 products did not pass the recovery test, which requires that the compressed product fully expand within 1 minute of hydration time.