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LIFECELL CORP

Last updated September 17, 2026

Information

Country: US
Address: 4 Millenium Way, Branchburg, NJ, 08876
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3016823837
DUNS Number: —

Catalogue (92)

Page 2 of 2

Device	Model / Reference	Registries	Class	Status
Strattice Reconstructive Tissue Matrix	0613009	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Perforated	2040002P	FDA UDI	Class II	Active
Conexa Reconstructive Tissue Matrix	0606004	FDA UDI	Class II	Unknown
ARTIA Reconstructive Tissue Matrix	08201097	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Perforated	1016002P	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix BPS	CON3006	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	08161097	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	CL1097	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	CXL1097	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	1525002ET	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	1020002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Laparoscopic	0608005	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix BPS	CON1006	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	1530002	FDA UDI	Class II	Active
Conexa Reconstructive Tissue Matrix	0303003	FDA UDI	Class II	Unknown
Strattice Reconstructive Tissue Matrix Laparoscopic	1010005	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	2540002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	2030002ET	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	06161097	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	2030002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	3030002ET	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	1016002ET	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	1620002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	2040002ET	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Laparoscopic	1016005	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	0816001	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Perforated	2025002P	FDA UDI	Class II	Active
Ltm-T Surgical Mesh	K080353	FDA 510(k)	Class II	Active
LTM-Perforated Surgical Mesh	K150712	FDA 510(k)	Class II	Active
HP Tissue Matrix	K142326	FDA 510(k)	Class II	Active
Ltm Wound Dressing	K082103	FDA 510(k)	U	Active
Lifecell Tissue Expander	K112534	FDA 510(k)	U	Active
REVOLVE ENVI 600 Advanced Adipose System	K193539	FDA 510(k)	Class II	Active
Ltn - Laparoscopic Surgical Mesh	K130817	FDA 510(k)	Class II	Active
Lifecell Dural Substitute Matrix	K061208	FDA 510(k)	Class II	Active
Revolve Envi 600 Advanced Adipose System	K163647	FDA 510(k)	Class II	Active
ARTIA Reconstructive Tissue Matrix Perforated	K162752	FDA 510(k)	Class II	Active
Allocraft Dbm	K052735	FDA 510(k)	Class II	Active
Ltm-Bps Surgical Mesh	K082176	FDA 510(k)	Class II	Active
Ltm-Rc Surgical Mesh	K071986	FDA 510(k)	Class II	Active
Lrtm Surgical Mesh	K070560	FDA 510(k)	Class II	Active
Ltm-Labaroscopic Surgical Mesh	K121289	FDA 510(k)	Class II	Active

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FDA Recalls (5)

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
Jul 13, 2011	Z-0178-2012	—	terminated	The use of Strattice for stoma reinforcement at the time of stoma creation is not within the product's cleared indications for use in the US market.
Sep 13, 2010	Z-0162-2011	—	terminated	Graft Jacket Xpress kits contain catheters that will expire or have already expired prior to the labeled expiration of the human tissue component of the product on the outer box.
Jul 12, 2010	Z-2623-2010	—	terminated	Mislabeled -One lot of product labeled as 8 cm x 8 cm were actually cut using a 6 cm x 6 cm template.
Oct 17, 2007	Z-1299-2008	—	terminated	Improper donor screening test; diagnostic test kits were used in lieu of a donor screening test kits for HBsAG and HBcAB (later re-testing with FDA-approved donor screening test found samples non-reactive for both Hepatitis B Surface Antigen and Hepatitis B Core IgM/IgG Antibody)
Oct 17, 2007	Z-1298-2008	—	terminated	Improper donor screening test; diagnostic test kits were used in lieu of a donor screening test kits for HBsAG and HBcAB (later re-testing with FDA-approved donor screening test found samples non-reactive for both Hepatitis B Surface Antigen and Hepatitis B Core IgM/IgG Antibody)