HomeUSAMedical High Technology International, Inc.

Medical High Technology International, Inc.

USA · Clearwater
✓ 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
64listed device types
Class I 30Class II 34Class III 0
plus 64 registration records and 1 510(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
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 States64 registration records, 1 510(k), 0 PMA, 40 excluded
Brazil0 confirmed, 5 excluded
Saudi Arabia0 confirmed, 6 excluded
Canada0 confirmed, 6 excluded
Manufacturer names merged into this page: High Technology, Inc.

Company information

Country
USA
City
Clearwater

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

11987 · K873580

FDA listed device types

showing 8 of 64
Diluent, Blood Cell 1Colorimeter, Photometer, Spectrophotometer For Clinical Use 1Acid, Lactic, Enzymatic Method 1Ferrozine (Colorimetric) Iron Binding Capacity 1Phosphomolybdate (Colorimetric), Inorganic Phosphorus 1Microscope, Inverted Stage, Tissue Culture 1Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use 1Electrode, Ion Selective (Non-Specified) 1

Registration details (sample)

MarketIdentifierNameClass / date
USK873580MHTI CT-SIM RADIATION THERAPY TREATMENT SIMULATOR1987-11-02

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