HomeItalyTHD SPA

THD SPA

Italy · Correggio Reggio Emilia
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Australia, Israel — 3 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
18listed device types
Class I 5Class II 13Class III 0
plus 21 registration records and 13 510(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
26active ARTG entries
Class I 9IIa 14IIb 1Class Is (sterile) 2
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
21registrations
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 States21 registration records, 13 510(k), 0 PMA, 1 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: THD SPA

Company information

Country
Italy
City
Correggio Reggio Emilia

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

22008
22009
12010
12011
12012
12013
12015
12017
12018
12020
12021

FDA listed device types

showing 8 of 18
Suture, Surgical, Absorbable, Polydioxanone 1Transducer, Ultrasonic, Diagnostic 1System, Imaging, Pulsed Echo, Ultrasonic 1Endoscope, Ac-Powered And Accessories 1System, Imaging, Pulsed Doppler, Ultrasonic 1Proctoscope 1Monitor, Esophageal Motility, Anorectal Motility, And Tube 1Suture, Absorbable, Synthetic, Polyglycolic Acid 1

Registration details (sample)

MarketIdentifierNameClass / date
USK211623THD Procto Software System2021-06-24
USK193512THD Procto Software System2020-01-26
USK180135THD Anopress with THD SensyProbe2018-03-08

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