HomeUSAMillennium Medical Technologies, Inc.

Millennium Medical Technologies, Inc.

USA · Pleasant Hill
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 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
8listed device types
Class I 6Class II 2Class III 0
plus 9 registration records and 6 510(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
TWTaiwanTFDA
pendingnot queried
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 States9 registration records, 6 510(k), 0 PMA, 19 excluded
Brazil0 confirmed, 4 excluded
Canada0 confirmed, 3 excluded
Manufacturer names merged into this page: MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx

Company information

Country
USA
City
Pleasant Hill

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

22002 · K020791
12003 · K031050
12008 · K081039
12017 · K170449
12022 · K210528

FDA listed device types

System, Suction, Lipoplasty 1System, Suction, Lipoplasty For Removal 1Motor, Surgical Instrument, Ac-Powered 1Syringe, Irrigating (Non Dental) 1Cannula, Surgical, General & Plastic Surgery 1Brush, Dermabrasion, Powered 1Instrument, Manual, Surgical, General Use 1Accessories, Catheter 1

Registration details (sample)

MarketIdentifierNameClass / date
USK210528IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit2022-03-16
USK170449Autoclavable Suction Jar with Luer Lock extension - 250, 500, 1,000, 2,000 and 3,000 ml, Autoclavable Suction Jar without Luer Lock extension - 1,500 and 2,500 ml, Sterile 1,500 and 2,500 Lids with Conical patient connection 6-10 and overflow protection2017-03-31
USK081039LIPO CANNULA2008-07-10

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