HomeUSARADIATION PRODUCTS DESIGN, INC.

RADIATION PRODUCTS DESIGN, INC.

USA · Albertville
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Taiwan, Australia, Israel — 4 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
22listed device types
Class I 20Class II 2Class III 0
plus 22 registration records and 9 510(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
4valid device licences
Class I 4
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
3active ARTG entries
Class I 3
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
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 States22 registration records, 9 510(k), 0 PMA, 37 excluded
Saudi Arabia0 confirmed, 1 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: RADIATION PRODUCTS DESIGN, INC.

Company information

Country
USA
City
Albertville

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

11979
61980 · K800760
12015 · K150382
12018 · K180027

FDA listed device types

showing 8 of 22
Lift, Patient, Non-Ac-Powered 1Protractor 1Device, Transfer, Patient, Manual 1Stains, Dye Solution 1Bed, Manual 1Stand, Infusion 1Caliper 1Shield, Eye, Radiological 1

Registration details (sample)

MarketIdentifierNameClass / date
USK180027ACCUSYTE 3D Fiducial Marker2018-07-18
USK150382Radio Therapy Treatment Chair2015-09-16
USK800760BITE BLOCK SYSTEM1980-05-28

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