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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 12 of 15

Device	Model / Reference	Registries	Class	Status
NeuroMatrix	CNC5025	FDA UDI	Class II	Active
RegenerOss	RGP0625	FDA UDI	Class II	Active
OssiMend BLOCK	MCCB1004	FDA UDI	Class II	Active
MaxxDerm+	XE304	FDA UDI	Class II	Active
SMARTGRAFT Granules	0114.113	FDA UDI	Class II	Active
Mem-Lok	RCM-ML2030	FDA UDI	Class II	Active
BoneSync BioActive	ABS-3500-20	FDA UDI	Class II	Active
OssiMend® Bioactive	MCCBA0506	FDA UDI	Class II	Active
BVital GENOSS Granules	BS-G040	FDA UDI	Class II	Active
OssiMend	MCC2020-1	FDA UDI	Class II	Active
BVital GENOSS Granules	BS-G020	FDA UDI	Class II	Active
MatrixFlex	CDMPP3040	FDA UDI	Class II	Active
BioMend	0103Z	FDA UDI	Class II	Active
Mem-Lok Pliable	PBLE-ML1520	FDA UDI	Class II	Active
OssiMend® Bioactive \| Strip	MCCBA0503	FDA UDI	Class II	Active
Symbios	32310008	FDA UDI	Class II	Unknown
Zimmer Collagen Tape	0100Z	FDA UDI	U	Active
OssiMend Putty	PS-MCCP10	FDA UDI	Class II	Active
PlatFORM CM Pad	CM78702	FDA UDI	Class II	Active
MaxxMem+	XP304	FDA UDI	Class II	Active
OSTEO-Flex	OSTEOF20x30	FDA UDI	Class II	Active
BIA-GEN Bioactive	CS-MCCBA2012	FDA UDI	Class II	Active
BoneSync BioActive	ABS-3500-05	FDA UDI	Class II	Active
CollaShield Extend	CSE20X30	FDA UDI	Class II	Active
NeoGenix XP Syringe	64097	FDA UDI	Class II	Active
PuraFILL	PFPLG625	FDA UDI	Class II	Active
AccuFuse	WMS10	FDA UDI	Class II	Active
Mem-Lok	RCM-ML1520	FDA UDI	Class II	Active
DuraMend-Onlay™	NDMO45	FDA UDI	Class II	Active
MinerOss XP Syringe	MINXP-SYR0.25	FDA UDI	Class II	Active
MatrixDerm Foam	BDDWDF2040	FDA UDI	U	Active
Augmatrix	M620-100-10	FDA UDI	Class II	Active
Reguarde	2030	FDA UDI	Class II	Active
Arthrex Nerve Wrap	ABS-6050W	FDA UDI	Class II	Active
DuraMatrix-Onlay Plus	DMOP13	FDA UDI	Class II	Active
OSTEO-Derm Enhanced	OSTEODE30x40	FDA UDI	Class II	Active
Stylos BA \| Putty	STYP002	FDA UDI	Class II	Active
X-GEN Granules	PMC1010	FDA UDI	Class II	Active
DuraMend™	NDM33	FDA UDI	Class II	Active
PLENA Graft 0.5	PMC0510	FDA UDI	Class II	Active
DuraMatrix Suturable	DMS33	FDA UDI	Class II	Active
BVital GENOSS Granules	BS-GL010	FDA UDI	Class II	Active
Zimmer Collagen Plug	0102Z	FDA UDI	U	Active
DuraMatrix Suturable	DMS22	FDA UDI	Class II	Active
PLENA Graft 0.5cc Syringe	PMCS05	FDA UDI	Class II	Active
DuraMatrix-Onlay Conform	DMOC45	FDA UDI	Class II	Active
BVital GENOSS Granules	BS-GL020	FDA UDI	Class II	Active
OssiGuide	PS-OG05	FDA UDI	Class II	Active
DuraMatrix-Onlay Conform	DMOC11	FDA UDI	Class II	Active
VIA Mend Putty	VMP0025	FDA UDI	Class II	Active

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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.