Is this your brand? Sign in to claim ownership.

LIFECELL CORP

Last updated September 17, 2026

Information

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

Catalogue (92)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
ARTIA Reconstructive Tissue Matrix	CS1097P	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	2040002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	0610008	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	0606002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	0516001	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Laparoscopic	2020005	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	5510009	FDA UDI	Class II	Active
Conexa Reconstructive Tissue Matrix	0404004	FDA UDI	Class II	Unknown
Strattice Reconstructive Tissue Matrix	0815009	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	CS1097	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	2025002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	2020002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	0608001	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	1535002ET	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Perforated	2540002P	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Perforated	1020002P	FDA UDI	Class II	Active
Conexa Reconstructive Tissue Matrix	0510004	FDA UDI	Class II	Unknown
Strattice Reconstructive Tissue Matrix	3030002	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	16201097	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix BPS	0314006	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Perforated	1535002P	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	1025002	FDA UDI	Class II	Active
Revolve Advanced Adipose System	RV0001	FDA UDI	Class II	Active
Conexa Reconstructive Tissue Matrix	0510003	FDA UDI	Class II	Unknown
Strattice Reconstructive Tissue Matrix BPS	1016006	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	2540002ET	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Laparoscopic	1620005	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Perforated	2030002P	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	1525002	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	CL1097P	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix BPS	0808006	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	1010002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	0616002	FDA UDI	Class II	Active
Conexa Reconstructive Tissue Matrix	0204004	FDA UDI	Class II	Unknown
ARTIA Reconstructive Tissue Matrix	16201097P	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	CM1097P	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	0808002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix	1016002	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	1620002ET	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix BPS	CON2006	FDA UDI	Class II	Active
Revolve ENVI 600 Advanced Adipose System	RV0001E600	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	10161097	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Perforated	1620002P	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	2025002ET	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix BPS	0416006	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Perforated	2020002P	FDA UDI	Class II	Active
Conexa Reconstructive Tissue Matrix	0505003	FDA UDI	Class II	Unknown
ARTIA Reconstructive Tissue Matrix	CXL1097P	FDA UDI	Class II	Active
ARTIA Reconstructive Tissue Matrix	CM1097	FDA UDI	Class II	Active
Strattice Reconstructive Tissue Matrix Extra Thick	2020002ET	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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)