LIFECELL CORP.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
16470981000306051LIFECELL CORP.1N2027-01-01ONE MILLENNIUM WAY BRANCHBURG NJ US 08876

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2083621563046382K163647Revolve Envi 600 Advanced Adipose SystemMUU2017-08-25
2083621363938590K162752ARTIA Reconstructive Tissue Matrix PerforatedFTM2017-02-24
2083621795014723K150712LTM-Perforated Surgical MeshFTM2015-07-02
2083621987176599K142326HP Tissue MatrixFTM2014-12-23
2083622049051054K130817LTN - LAPAROSCOPIC SURGICAL MESHOXK2013-04-17
2083621002606824K120902GID 700MUU2012-08-15
2083621160324222K082176LTM-BPS SURGICAL MESHFTM2008-11-14
2083621916353224K070560LRTM SURGICAL MESHFTM2007-06-11
2083621825500457BK220721
2083622004931128BK220695
2083621218928444

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FTM52017-02-24
MUU22017-08-25
OXK12013-04-17

PMN#