HomeUSALifecell Corporation

Lifecell Corporation

USA · Branchburg
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Canada, Taiwan, South Korea, Australia, Israel — 6 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
5listed device types
Class I 0Class II 5Class III 0
plus 18 registration records and 15 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
3 including historic records
TWTaiwanTFDA
1valid device licences
Class II 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
Import 1
AUAustraliaTGA ARTG
1active ARTG entries
IIa 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
5registrations
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States18 registration records, 15 510(k), 0 PMA
Manufacturer names merged into this page: LIFECELL CORP · LIFECELL CORP. · LIFECELL CORPORATION

Company information

Country
USA
City
Branchburg

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12005
32007
32008
22012
12013
12014
12015
22017
12020

FDA listed device types

Barrier, Animal Source, Intraoral 1Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery 1Mesh, Surgical, Collagen, Large Abdominal Wall Defects 1Mesh, Surgical 1Lipoaspirate Washing System For Aesthetic Body Contouring 1

Registration details (sample)

MarketIdentifierNameClass / date
USK193539REVOLVE ENVI 600 Advanced Adipose System2020-05-28
USK163647Revolve Envi 600 Advanced Adipose System2017-08-25
USK162752ARTIA Reconstructive Tissue Matrix Perforated2017-02-24

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