HomeUSALife-Tech, Inc.

Life-Tech, Inc.

USA · Houston
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 2 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
14510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 14 510(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
27active device licences
Class II 27
30 including historic records
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
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 States0 registration records, 14 510(k), 0 PMA, 246 excluded
Brazil0 confirmed, 62 excluded
Saudi Arabia0 confirmed, 19 excluded
Canada27 confirmed, 37 excluded
Manufacturer names merged into this page: LIFE-TECH INC.

Company information

Country
USA
City
Houston

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
12006
12007
42008
12009
32010
22011
12012

Registration details (sample)

MarketIdentifierNameClass / date
USK120234EZONO 30002012-04-19
USK111355ECHOBRIGHT2011-09-16
USK102813EZONO 30002011-06-30
CA3283UROLAB JANUS PATIENT UNITClass II
CA5436VIDEO URODYNAMIC SYSTEMClass II
CA5437ABDOMINAL PRESSURE CATHETERClass II

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