HomeUSASDI DIAGNOSTICS, INC.

SDI DIAGNOSTICS, INC.

USA · South Easton
✓ 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
3listed device types
Class I 1Class II 2Class III 0
plus 6 registration records and 10 510(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 States6 registration records, 10 510(k), 0 PMA, 5 excluded
Brazil0 confirmed, 4 excluded
Saudi Arabia0 confirmed, 2 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: SDI DIAGNOSTICS, INC.

Company information

Country
USA
City
South Easton

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

11993
12000
12001
12002
12003
12004
22007
12010
12016

FDA listed device types

Filter, Bacterial, Breathing-Circuit 1Spirometer, Diagnostic 1Mouthpiece, Breathing 1

Registration details (sample)

MarketIdentifierNameClass / date
USK150515IQSense Flow Sensor Mouthpiece2016-01-12
USK092813ASTRASONIC SPIROMETER, MODEL 29-80002010-07-16
USK061571ASTRA 3002007-01-31

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